406 results match your criteria Glaucoma Secondary Congenital


Risk of aphakic glaucoma after pars plana-lensectomy with and without removal of the peripheral lens capsule.

Eye (Lond) 2019 Apr 10. Epub 2019 Apr 10.

Eye Center, Medical Center, Medical Faculty, University of Freiburg, Freiburg, Germany.

Background: The etiology of aphakic glaucoma is unclear. It has been suggested that remaining lens epithelium releases cytokines transducing trabecular meshwork cells. Therefore, we compared two cohorts of children undergoing lensectomy. Read More

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http://dx.doi.org/10.1038/s41433-019-0435-xDOI Listing

Early results of micropulse transscleral cyclophotocoagulation for the treatment of glaucoma.

Eur J Ophthalmol 2019 Apr 2:1120672119839303. Epub 2019 Apr 2.

1 Department of Ophthalmology and Visual Science, Yale School of Medicine, New Haven, CT, USA.

Purpose:: To describe our clinical experience with the efficacy and safety of micropulse transscleral cyclophotocoagulation as a treatment for glaucoma.

Methods:: In this retrospective case series, we reviewed the charts of 95 consecutive patients with various glaucoma subtypes who underwent micropulse transscleral cyclophotocoagulation. Patients were offered micropulse transscleral cyclophotocoagulation if they had perimetric glaucoma refractory to intraocular pressure-lowering topical medications and who were poor candidates for traditional filtering surgery. Read More

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http://dx.doi.org/10.1177/1120672119839303DOI Listing
April 2019
11 Reads

The role of primary intraocular lens implantation in the risk of secondary glaucoma following congenital cataract surgery: A systematic review and meta-analysis.

PLoS One 2019 1;14(4):e0214684. Epub 2019 Apr 1.

Department of Ophthalmology, Xiangya Hospital, Central South University, Changsha, Hunan, China.

Objective: This meta-analysis aims to evaluate the incidence of secondary glaucoma in patients under the age of 2 years who underwent congenital cataract surgery with or without primary intraocular lens (IOL) implantation.

Methods: An electronic literature search was performed in Medline, EMBASE, and Web of Science databases to retrieve studies between January 2011 and November 2018. Patients with congenital cataract who did primary IOL implantation, aphakia, or secondary IOL implantation followed by receiving extraction surgery were included in this study. Read More

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0214684PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443152PMC

Oculo-Facio-Cardio-Dental Syndrome: A Case Report about a Rare Pathological Condition.

Int J Environ Res Public Health 2019 Mar 14;16(6). Epub 2019 Mar 14.

Institute of Endodontics, Institute of Integrated Clinical Practice, Institute of Experimental Pathology,Institute for Clinical and Biomedical Research (iCBR), Area of Environment Genetics and Oncobiology(CIMAGO), CNC.IBILI, Faculty of Medicine, University of Coimbra, Avenida Bissaya Barreto,3000-075 Coimbra, Portugal.

(1) Background: Oculo-facio-cardio-dental (OFCD) syndrome is a rare pathological condition with an X-linked dominant trait that only occurs in females; no males are born with OFCD syndrome. This syndrome is characterized by congenital cataracts with secondary glaucoma ocular defects, ventricular and atrial septal defects, or mitral valve prolapses. Facial traits are a long narrow face and a high nasal bridge with a bifid nasal tip. Read More

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http://dx.doi.org/10.3390/ijerph16060928DOI Listing

Secondary Congenital Glaucoma Associated With Retro-orbital Infantile Hemangioma: A Masquerade Syndrome.

J Glaucoma 2019 Mar 6. Epub 2019 Mar 6.

University Hospital Nord, Chemin des Bourrely, Marseille, France.

Purpose: The main purpose of this study was to describe a unique case of retro-orbital infantile hemangioma (IH) simulating a congenital glaucoma requiring prompt management with systemic propranolol.

Study Design: This was a case report.

Results: A 2-month-old white female was referred to our department of ophthalmology for progressive, unilateral protrusion of the left eye associated with epiphora. Read More

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http://dx.doi.org/10.1097/IJG.0000000000001227DOI Listing
March 2019
7 Reads

Launching a paradigm for first and redo-surgery in primary congenital glaucoma: institutional experience.

Int J Ophthalmol 2019 18;12(2):226-234. Epub 2019 Feb 18.

Mansoura Ophthalmic Center, Faculty of Medicine, Mansoura University, Mansoura 35516, Egypt.

Aim: To evaluate the outcome of the initial and the redo-surgeries for primary congenital glaucoma (PCG) correlated to its degree of severity.

Methods: A retrospective study involved patients with PCG presented between 2010 and 2018. Medical records were reviewed to assess the degree of the preoperative severity according to the intraocular pressure (IOP), corneal diameter and corneal edema. Read More

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http://dx.doi.org/10.18240/ijo.2019.02.07DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376225PMC
February 2019
1 Read

Profile of childhood glaucoma at a tertiary center in South India.

Indian J Ophthalmol 2019 Mar;67(3):358-365

VST Glaucoma Center, L V Prasad Eye Institute, Banjara Hills, Hyderabad, Telangana, India.

Purpose: To describe the prevalence of various types of childhood glaucomas, their clinical features and treatment methods.

Methods: We prospectively included consecutive children with glaucoma presenting to glaucoma clinic for the first time between March 2013 and May 2014. We classified childhood glaucomas as per the classification proposed by Congenital Glaucoma Research Network. Read More

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http://dx.doi.org/10.4103/ijo.IJO_786_18DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407385PMC

Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma.

JAMA Ophthalmol 2019 Jan 17. Epub 2019 Jan 17.

Department of Ophthalmology, Flinders University, Flinders Medical Centre, Adelaide, Australia.

Importance: Both primary and secondary forms of childhood glaucoma have many distinct causative mechanisms, and in many cases a cause is not immediately clear. The broad phenotypic spectrum of secondary glaucoma, particularly in individuals with variants in FOXC1 or PITX2 genes associated with Axenfeld-Rieger syndrome, makes it more difficult to diagnose patients with milder phenotypes. These cases are occasionally classified and managed as primary congenital glaucoma. Read More

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http://archopht.jamanetwork.com/article.aspx?doi=10.1001/jam
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http://dx.doi.org/10.1001/jamaophthalmol.2018.5646DOI Listing
January 2019
9 Reads

Syndromic Multisuture Craniosynostosis With Associated Anterior Segment Dysgenesis, Optic Nerve Hypoplasia, and Congenital Glaucoma.

Cleft Palate Craniofac J 2018 Dec 25:1055665618820481. Epub 2018 Dec 25.

1 Division of Plastic Surgery, Baylor College of Medicine, Houston, TX, USA.

Patients with craniosynostosis with subnormal vision due to papilledema and/or exposure-related corneal decompensation are well documented in the literature; however, there is only a single prior documented case of vision compromise secondary to anterior segment dysgenesis and glaucoma in this patient population. This report highlights a case of syndromic craniosynostosis with advanced corneal decompensation and anterior segment dysgenesis that was masked and ultimately delayed the diagnosis of congenital glaucoma. Read More

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http://dx.doi.org/10.1177/1055665618820481DOI Listing
December 2018
2 Reads

Efficacy and safety of vitrectomy for congenital cataract surgery: a systematic review and meta-analysis based on randomized and controlled trials.

Acta Ophthalmol 2019 May 22;97(3):233-239. Epub 2018 Nov 22.

Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Key Laboratory of Ophthalmology and Visual Sciences, Beijing Tongren Hospital of Capital Medical University, Beijing, China.

Purpose: To explore the effectiveness and safety of vitrectomy for congenital cataract surgery.

Methods: We searched PubMed, Science Direct, The Cochrane Library, China National Knowledge Infrastructure and the Wanfang Database. Two researchers extracted data and assessed paper quality independently. Read More

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http://doi.wiley.com/10.1111/aos.13974
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http://dx.doi.org/10.1111/aos.13974DOI Listing
May 2019
14 Reads
2.844 Impact Factor

LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant.

Am J Med Genet A 2019 Jan 18;179(1):104-112. Epub 2018 Dec 18.

Pediatric Cardiology and Arrhythmology Unit, Department of Pediatric Cardiology and Cardiac Surgery, IRCCS-Bambino Gesù Children Hospital and Research Institute, Rome, Italy.

Recessive variants in LTBP2 are associated with eye-restricted phenotypes including (a) primary congenital glaucoma and (b) microspherophakia/megalocornea and ectopia lentis with/without secondary glaucoma. Nosology of LTBP2 pathology in humans is apparently in contrast with the consolidated evidence of a wide expression of this gene in the developing embryo. Accordingly, in previously published patients with LTBP2-related eye disease, additional extraocular findings have been occasionally reported and include, among others, high-arched palate, tall stature, and variable cardiac involvement. Read More

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http://doi.wiley.com/10.1002/ajmg.a.10
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http://dx.doi.org/10.1002/ajmg.a.10DOI Listing
January 2019
19 Reads

Systemic Associations of Childhood Glaucoma: A Review.

J Pediatr Ophthalmol Strabismus 2018 Nov;55(6):397-402

Purpose: To review systemic associations of childhood glaucoma.

Methods: Patients younger than 15 years and diagnosed as having glaucoma were divided into four groups: isolated primary congenital glaucoma, glaucoma with other congenital ocular anomalies, congenital glaucoma with known systemic diseases, and secondary glaucoma. Prevalence and type of systemic associations in each group were studied. Read More

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https://www.healio.com/doiresolver?doi=10.3928/01913913-2018
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http://dx.doi.org/10.3928/01913913-20180905-01DOI Listing
November 2018
11 Reads
0.731 Impact Factor

Medical Management of Children With Congenital/Infantile Cataract Associated With Microphthalmia, Microcornea, or Persistent Fetal Vasculature.

J Pediatr Ophthalmol Strabismus 2019 Jan 26;56(1):43-49. Epub 2018 Oct 26.

Purpose: To report the surgical outcomes of children with cataract associated with microphthalmia, microcornea, or persistent fetal vasculature (MMP) and children with isolated cataract.

Methods: The study included 111 children (cataract associated with MMP: n = 25) who underwent cataract surgery at younger than 16 years. Exclusion criteria were duration of follow-up less than 5 years, intraindividual differences in age at surgery, eye disorders other than MMP, secondary cataract, and syndromal diseases. Read More

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https://www.healio.com/doiresolver?doi=10.3928/1081597X-2018
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http://dx.doi.org/10.3928/1081597X-20180924-01DOI Listing
January 2019
12 Reads

Preoperative biometry data of eyes with unilateral congenital cataract.

J Cataract Refract Surg 2018 Oct;44(10):1198-1202

From the Department of Ophthalmology, Semmelweis University, Budapest, Hungary.

Purpose: To investigate the differences in biometry data of eyes with unilateral congenital cataract and the contralateral normal eyes in pediatric patients.

Setting: Pediatric Ophthalmology Division, Ophthalmology Department, Semmelweis University in Budapest, Hungary.

Design: Retrospective case series. Read More

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http://dx.doi.org/10.1016/j.jcrs.2018.06.054DOI Listing
October 2018
2 Reads

Phenotype-genotype correlations and emerging pathways in ocular anterior segment dysgenesis.

Hum Genet 2018 Sep 21. Epub 2018 Sep 21.

Eye Genetics Research Unit, The Children's Hospital at Westmead, Save Sight Institute, Children's Medical Research Institute, The University of Sydney, Sydney, NSW, 2145, Australia.

Disorders of the anterior segment of the eye encompass a variety of clinical presentations including aniridia, Axenfeld and Rieger anomalies, primary congenital glaucoma, Peters anomaly, as well as syndromal associations. These conditions have a significant impact on vision due to disruption of the visual axis, and also secondary glaucoma which occurs in over 50% of patients. Ocular anterior segment disorders occur due to a complex interplay of developmental, embryological and genetic factors, and often have phenotypic overlaps and genetic heterogeneity. Read More

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http://dx.doi.org/10.1007/s00439-018-1935-7DOI Listing
September 2018
1 Read

Choroidal Detachment and Increased Intraocular Pressure in a Case of Secondary Pulmonary Hypertension.

J Glaucoma 2019 Jan;28(1):e1-e4

The First Hospital of Lanzhou University.

Purpose: To report a case of secondary pulmonary hypertension, choroidal detachment, and increased intraocular pressure (IOP) in a patient with a congenital ventricular septal defect.

Methods: This is a case report.

Patient: A 36-year-old man with congenital ventricular septal defect developed dilated and congested conjunctival and episcleral veins, high IOP, and choroidal detachment. Read More

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http://dx.doi.org/10.1097/IJG.0000000000001090DOI Listing
January 2019
4 Reads

Long-term results of secondary intraocular lens implantation in children under 30 months of age.

Eye (Lond) 2018 12 28;32(12):1858-1863. Epub 2018 Aug 28.

Sant Joan de Déu Hospital, Barcelona, Spain.

Purpose: To report the long-term outcome of early secondary intraocular lens (IOL) implantation following congenital cataract extraction in a large number of eyes.

Methods: Data of aphakic children under 30 months of age who underwent secondary IOL implantation and had at least one year of follow-up after the surgery was reviewed. In all of the patients, a foldable three-piece acrylic IOL was implanted in the ciliary sulcus by the same surgeon using the same technique. Read More

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http://www.nature.com/articles/s41433-018-0191-3
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http://dx.doi.org/10.1038/s41433-018-0191-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292907PMC
December 2018
19 Reads

Risk factors for flat anterior chamber after glaucoma filtration surgery.

Int J Ophthalmol 2018 18;11(8):1322-1329. Epub 2018 Aug 18.

Department of Ophthalmology, the Third Affiliated Hospital, Chongqing Medical University, Chongqing 400016, China.

Aim: To investigate the incidence rate and risk factors for grade III flat anterior chamber (FAC) after glaucoma filtration surgery based on 5-year data.

Methods: Patients who underwent glaucoma filtration surgery in Daping hospital from January 2009 to December 2013 were enrolled in this retrospective study. The incidence of grade III FAC following glaucoma filtration surgery was determined. Read More

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http://dx.doi.org/10.18240/ijo.2018.08.12DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090123PMC
August 2018
9 Reads
0.500 Impact Factor

Use of an onlay corneal lamellar graft for brittle cornea syndrome.

BMJ Case Rep 2018 Aug 16;2018. Epub 2018 Aug 16.

Moorfields Eye Hospital NHS Foundation Trust, London, UK.

Brittle cornea syndrome (BCS1 OMIM #229200, BCS2 #614170) is a rare autosomal recessive condition characterised by diffuse thinning and fragility of the cornea. Affected individuals are at risk of globe rupture and blindness after relatively minor eye trauma. We describe a 9-year-old girl with BCS1, already blind in one eye following trauma, who had a 14 mm diameter corneoscleral onlay graft to her contralateral eye to reduce gross irregular corneal astigmatism and potentially to reduce further risk from accidental injury. Read More

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http://casereports.bmj.com/lookup/doi/10.1136/bcr-2017-22382
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http://dx.doi.org/10.1136/bcr-2017-223824DOI Listing
August 2018
30 Reads

New classification system for pediatric glaucoma: implications for clinical care and a research registry.

Curr Opin Ophthalmol 2018 Sep;29(5):385-394

Sidney Kimmel Medical College at Thomas Jefferson University.

Purpose Of Review: The Childhood Glaucoma Research Network (CGRN) has created a new classification system for childhood glaucoma that has become the first International Consensus Classification. The purpose of this review is to present this classification system and share its use to date.

Recent Findings: The diagnoses of the classification system include glaucoma and glaucoma suspect. Read More

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http://dx.doi.org/10.1097/ICU.0000000000000516DOI Listing
September 2018
44 Reads

Outcomes of Silicone Ahmed Glaucoma Valve Implantation in Refractory Pediatric Glaucoma.

J Glaucoma 2018 Sep;27(9):769-775

VST Glaucoma Center.

Purpose: The purpose of this study was to report the outcomes of Silicone Ahmed Glaucoma Valve (AGV) implantation in the management of refractory pediatric glaucoma.

Methods: Between 2007 and 2015, 76 eyes of 64 children aged 16 years or younger underwent AGV implantation. We included 65 eyes of 53 children with follow up ≥6 months; 24 eyes had primary congenital glaucoma (PCG) and 41 eyes had secondary pediatric glaucoma (SPG). Read More

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http://Insights.ovid.com/crossref?an=00061198-201809000-0000
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http://dx.doi.org/10.1097/IJG.0000000000001032DOI Listing
September 2018
24 Reads

Catheter-assisted 360-Degree Trabeculotomy for Congenital Glaucoma.

J Glaucoma 2018 Jul;27(7):572-577

Department of Ophthalmology, University Medical Center Mainz, Mainz.

Purpose: To determine feasibility, efficacy, and safety of ab externo 360-degree trabeculotomy with illuminated microcatheter for congenital glaucoma.

Patients And Methods: The postoperative results of 36 eyes in 23 consecutive patients who underwent 360-degree trabeculotomy for primary congenital glaucoma (PCG) or secondary congenital glaucoma using an illuminated microcatheter were retrospectively analyzed. Success criteria were defined as intraocular pressure (IOP) ≤18 mm Hg without (complete success) and with medication (qualified success). Read More

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http://dx.doi.org/10.1097/IJG.0000000000000966DOI Listing
July 2018
1 Read

Effect of Exogenous Alpha-B Crystallin on the Structures and Functions of Trabecular Meshwork Cells.

J Ophthalmol 2018 17;2018:7875318. Epub 2018 Apr 17.

Department of Ophthalmology, Peking University People's Hospital, Eye diseases and Optometry Institute, Beijing Key Laboratory of Diagnosis and Therapy of Retina and Choroid Diseases, College of Optometry, Peking University Health Science Center, Beijing, China.

Purpose: Secondary open-angle glaucoma may develop as a postoperative complication of early childhood cataract surgery. Its mechanism is poorly understood. Surgical removal of cataracts is typically incomplete, and we estimate that this disease is associated with alpha-B crystallin (CRYAB) secreted from the retained lens material. Read More

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http://dx.doi.org/10.1155/2018/7875318DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932433PMC
April 2018
1 Read

Childhood glaucoma profile in Dakahelia, Egypt: a retrospective study.

Int J Ophthalmol 2018 18;11(4):674-680. Epub 2018 Apr 18.

Community and Public Health Department, Faculty of Medicine, Mansoura University, Mansoura 35516, Egypt.

Aim: To analyze childhood glaucoma regarding its demographics, presentations, different causes and surgical modalities used among patients in Dakahelia and to apply the Childhood Glaucoma Research Network (CGRN) classification retrospectively to evaluate its convenience.

Methods: A retrospective study in which the medical files of all glaucoma patients <16 years old presented to Mansoura Ophthalmic Center, Mansoura University from 2014 to 2017, were retrieved and analyzed. Collected data included: age, gender, laterality, visual acuity (VA), refraction, intraocular pressure (IOP), corneal diameter, cup-disc ratio, types and number of surgeries and antiglaucomatous drugs (AGD) at the first and last visit. Read More

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http://dx.doi.org/10.18240/ijo.2018.04.23DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902376PMC
April 2018
4 Reads

Ocular Decompression Retinopathy : A Case Series.

Nepal J Ophthalmol 2017 07;9(18):194-198

Introduction: Ocular decompression retinopathy (ODR) is a relatively rare entity with variable prognosis depending on extent and pre-existing condition. This article describes profile of two cases with a brief review of the condition.

Case Report: Case 1 highlights extensive choroidal detachment with subhyaloid haemorrhage and multiple intra-retinal hemorrhages in the posterior pole seen on first post-operative day in a 6 year old child with congenital glaucoma who underwent Trab & Trab. Read More

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https://www.nepjol.info/index.php/NEPJOPH/article/view/19269
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http://dx.doi.org/10.3126/nepjoph.v9i2.19269DOI Listing
July 2017
8 Reads

Temporary Piggyback Intraocular Lens Implantation Versus Single Intraocular Lens Implantation in Congenital Cataracts: Long-Term Clinical Outcomes.

Invest Ophthalmol Vis Sci 2018 04;59(5):1822-1827

Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

Purpose: To report the long-term results of temporary piggyback IOL implantation in congenital cataract and to compare the clinical outcomes of temporary piggyback IOL with those of single IOL implantation.

Methods: This is a retrospective, comparative, interventional study. The medical records of all consecutive patients who underwent cataract extraction and single or temporary piggyback IOL implantation within the first 3 years of life from 1999 to 2013 at Samsung Medical Center were reviewed. Read More

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http://iovs.arvojournals.org/article.aspx?doi=10.1167/iovs.1
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http://dx.doi.org/10.1167/iovs.17-23684DOI Listing
April 2018
4 Reads

Pathophysiology and management of glaucoma associated with phakomatoses.

J Neurosci Res 2019 Jan 1;97(1):57-69. Epub 2018 Apr 1.

Illinois Eye and Ear Infirmary, Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois.

The phakomatoses, encephalotrigeminal angiomatosis (ETA; Sturge-Weber Syndrome), neurofibromatosis type 1 (NF1 or von Recklinghausen disease), Von Hippel-Lindau (VHL) disease, tuberous sclerosis (TSC), oculodermal melanocytosis (ODM), and phakomatosis pigmentovascularis are a group of neurocutaneous disorders that have characteristic systemic and ocular manifestations. Through many different mechanisms, they may cause glaucomatous damage of the optic nerve and subsequent vision loss varying from mild to severe. Glaucoma commonly affects patients with ETA (43-72%), orbito-facial NF1 (23-50%), and ODM (10%). Read More

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http://doi.wiley.com/10.1002/jnr.24241
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http://dx.doi.org/10.1002/jnr.24241DOI Listing
January 2019
11 Reads

Clinical outcomes of Ahmed glaucoma valve implantation in pediatric glaucoma.

Eur J Ophthalmol 2019 Jan 27;29(1):44-51. Epub 2018 Mar 27.

1 Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Purpose:: To evaluate the outcomes of Ahmed glaucoma valve implantation in refractory primary congenital glaucoma as well as primary procedure in aphakic glaucoma.

Method:: In this retrospective study, medical records of patients who underwent Ahmed glaucoma valve implantation for refractory glaucoma and aphakic glaucoma were reviewed. Primary outcome measures were the surgical success defined as intraocular pressure ≤21 mm Hg and decreased ≥20% and no secondary glaucoma surgery. Read More

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http://dx.doi.org/10.1177/1120672118761332DOI Listing
January 2019
6 Reads

Glaucoma With Crouzon Syndrome.

J Glaucoma 2018 Jun;27(6):e110-e112

King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

Background: Crouzon syndrome is the most common form of craniosynostosis, and mutations in the fibroblast growth factor receptor 2 and 3 (FGFR2 and FGFR3) genes are implicated in its pathogenesis.

Observation: A 10-year-old female patient with Crouzon syndrome and congenital glaucoma treated with trabeculectomy and ocular hypotensive medications was examined. The patient had proptosis, exposure keratopathy, megalocornea, thin central corneal thickness, a shallow anterior chamber, mild anterior subcapsular cataract, and a cup-to-disc ratio of 0. Read More

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http://Insights.ovid.com/crossref?an=00061198-900000000-9847
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http://dx.doi.org/10.1097/IJG.0000000000000946DOI Listing
June 2018
23 Reads

Angle closure glaucoma in congenital ectropion uvea.

Am J Ophthalmol Case Rep 2018 Jun 9;10:215-220. Epub 2018 Mar 9.

Department of Ophthalmology and Visual Sciences, University of Michigan, United States.

Purpose: Congenital ectropion uvea is a rare anomaly, which is associated with open, but dysplastic iridocorneal angles that cause childhood glaucoma. Herein, we present 3 cases of angle-closure glaucoma in children with congenital ectropion uvea.

Observations: Three children were initially diagnosed with unilateral glaucoma secondary to congenital ectropion uvea at 7, 8 and 13 years of age. Read More

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https://linkinghub.elsevier.com/retrieve/pii/S24519936173002
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http://dx.doi.org/10.1016/j.ajoc.2018.03.009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854872PMC
June 2018
9 Reads

RETINAL NEOVASCULARIZATION FROM A PATIENT WITH CUTIS MARMORATA TELANGIECTATICA CONGENITA.

Retin Cases Brief Rep 2018 Mar 14. Epub 2018 Mar 14.

Department of Ophthalmology, Henry Ford Hospital, Detroit, Michigan.

Purpose: To report a rare case of peripheral retinal neovascularization in a patient diagnosed with cutis marmorata telangiectatica congenita (CMTC).

Methods: Observational case report.

Results: A 16-year-old girl was referred to clinic for retinal evaluation. Read More

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http://dx.doi.org/10.1097/ICB.0000000000000736DOI Listing
March 2018
3 Reads

Trabeculectomy with Ologen implant versus mitomycin C in congenital glaucoma secondary to Sturge Weber Syndrome.

Int J Ophthalmol 2018 18;11(2):251-255. Epub 2018 Feb 18.

Department of Ophthalmology, Ain Shams University, Cairo 11995, Egypt.

Aim: To compare the efficacy and safety of collagen matrix implant [Ologen (OLO) implant] versus mitomycin C (MMC) with subscleral trabeculectomy (SST) for the surgical treatment of congenital glaucoma (CG) in Sturge-Weber Syndrome (SWS).

Methods: A prospective comparative randomized study of 20 eyes of 16 patients with CG associated with SWS was divided into two groups. The first group (MMC Group) included 10 eyes that were subjected to SST with MMC. Read More

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http://dx.doi.org/10.18240/ijo.2018.02.12DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824080PMC
February 2018
2 Reads

Microcatheter-assisted Trabeculotomy Versus 2-site Trabeculotomy With the Rigid Probe Trabeculotome in Primary Congenital Glaucoma.

J Glaucoma 2018 Apr;27(4):371-376

Ophthalmology Department, Cairo University Faculty of Medicine, Cairo, Egypt.

Purpose: The purpose of this study was to compare the outcomes of microcatheter-assisted trabeculotomy to circumferential trabeculotomy using the rigid probe trabeculotome in primary congenital glaucoma.

Methods: This retrospective study was performed in an institutional setting. The medical records of primary congenital glaucoma patients who underwent circumferential trabeculotomy (≥270 degrees incised) using Glaucolight-illuminated microcatheter or a rigid probe trabeculotome were reviewed. Read More

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http://Insights.ovid.com/crossref?an=00061198-201804000-0001
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http://dx.doi.org/10.1097/IJG.0000000000000892DOI Listing
April 2018
2 Reads

[Clinical effects of pediatric penetrating keratoplasty for congenital corneal opacity].

Zhonghua Yan Ke Za Zhi 2017 Dec;53(12):941-946

Beijing Aier-Intech Eye Hospital, Beijing 100021, China.

To report the clinical results of pediatric penetrating keratoplasty (PKP) in patients under 3 years old with congenital corneal opacity. Retrospective study. Sixteen eyes of 12 patients who were treated with PKP in Aier Eye Hospital Group from June 2009 to December 2016 were enrolled in this study. Read More

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http://dx.doi.org/10.3760/cma.j.issn.0412-4081.2017.12.011DOI Listing
December 2017

Outcomes of Infantile-Onset Glaucoma Associated With Port Wine Birthmarks and Other Periocular Cutaneous Vascular Malformation.

Asia Pac J Ophthalmol (Phila) 2018 Mar-Apr;7(2):95-98. Epub 2017 Dec 27.

Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL.

Purpose: The incidence of infantile-onset secondary glaucoma associated with periocular cutaneous vascular malformations is high and the outcomes of these glaucomatous eyes have anecdotally been poor. The purpose of this study was to determine the anatomic and visual outcomes of affected eyes.

Design: Retrospective case series. Read More

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http://dx.doi.org/10.22608/APO.2017447DOI Listing
May 2018
23 Reads

A Case of Advanced Glaucoma with Increased Episcleral Venous Pressure in a 17-Year-Old with Eisenmenger Syndrome.

Case Rep Ophthalmol Med 2017 23;2017:5808047. Epub 2017 Oct 23.

Mater Dei Hospital, Msida, Malta.

Eisenmenger syndrome refers to reversal of shunt and central cyanosis due to pulmonary hypertension induced by congenital heart disease with a large systemic-to-pulmonary shunt. We report a case of a 17-year-old man with Eisenmenger syndrome who presented with gradual deterioration in visual acuity and was diagnosed with advanced secondary open angle glaucoma. There have been reports of patients suffering from thrombosis due to hyperviscosity associated with this syndrome; however, to our knowledge, the association of secondary open angle glaucoma with Eisenmenger syndrome has not yet been documented. Read More

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http://dx.doi.org/10.1155/2017/5808047DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5672606PMC
October 2017
18 Reads

Microphthalmia, Dermal Aplasia, and Sclerocornea Syndrome: Endoscopic Cyclophotocoagulation in the Management of Congenital Glaucoma.

J Glaucoma 2018 Jan;27(1):e7-e10

Departments of Ophthalmology.

Purpose: To report on the use of endoscopic cyclophotocoagulation (ECP) to treat congenital glaucoma in a triple X female with microphthalmia, dermal aplasia, and sclerocornea (MIDAS) syndrome.

Observations: The patient demonstrated linear streaks on the face and neck consistent with dermal aplasia. The corneas were scleralized with ectatic areas of corneal thinning, and the eyes were microphthalmic. Read More

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http://Insights.ovid.com/crossref?an=00061198-900000000-9859
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http://dx.doi.org/10.1097/IJG.0000000000000812DOI Listing
January 2018
6 Reads

Surgical Outcome of Congenital Cataract in Eyes With Microcornea.

J Pediatr Ophthalmol Strabismus 2018 Jan 9;55(1):30-36. Epub 2017 Oct 9.

Purpose: To report the intraoperative and postoperative outcomes of congenital cataract surgery in eyes with microcornea.

Methods: In this retrospective, interventional, comparative case series, the authors reviewed 47 eyes of 26 children with microcornea and congenital cataract (21 bilateral and 5 unilateral) who underwent lens aspiration with primary posterior capsulectomy and anterior vitrectomy between 2008 and 2014 with a minimum follow-up period of 6 months. Demographic profiles and systemic and ocular features were documented. Read More

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http://www.healio.com/doiresolver?doi=10.3928/01913913-20170
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http://dx.doi.org/10.3928/01913913-20170703-13DOI Listing
January 2018
6 Reads

Outcomes of cataract surgery in children with persistent hyperplastic primary vitreous.

Eur J Ophthalmol 2018 Mar 14;28(2):193-197. Epub 2017 Sep 14.

Department of Ophthalmology, Advanced Eye Center, Post Graduate Institute of Medical Education and Research, Chandigarh - India.

Purpose: To evaluate postoperative outcomes of cataract surgery in children with persistent hyperplastic primary vitreous (PHPV) and factors affecting outcomes.

Methods: We analyzed 29 eyes of 28 children with PHPV presenting at a tertiary care center in northern India. All eyes underwent phacoaspiration followed by primary posterior capsulotomy with or without cauterization of persistent fetal vasculature under general anesthesia. Read More

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http://dx.doi.org/10.5301/ejo.5001017DOI Listing
March 2018
6 Reads
1.060 Impact Factor

The genetics of congenital aniridia-a guide for the ophthalmologist.

Surv Ophthalmol 2018 Jan - Feb;63(1):105-113. Epub 2017 Sep 18.

Department of Ophthalmology, Oslo University Hospital, Oslo, Norway; Faculty of Health and Social Sciences, National Centre for Optics, Vision and Eye Care, University College of Southeast Norway, Kongsberg, Norway; Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.

Congenital aniridia is a rare panocular disease caused by fundamental disturbances in the development of the eye, characterized primarily by hypoplasia of the iris and macula. Severe secondary complications such as keratopathy, cataract, and glaucoma are common and often lead to considerable visual impairment or blindness. Many complications in aniridia patients are difficult to treat and present a challenge for the ophthalmologist. Read More

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http://dx.doi.org/10.1016/j.survophthal.2017.09.004DOI Listing
December 2017
10 Reads

Diagnostic impact of anterior segment angiography of limbal stem cell insufficiency in PAX6-related aniridia.

Clin Anat 2018 Apr 1;31(3):392-397. Epub 2018 Feb 1.

Department of Ophthalmology, Saarland University Medical Center UKS, Homburg/Saar, Kirrbergerstr, 100, Homburg, Saar, 66424, Germany.

PAX6 is a master gene of ocular development and postnatal ocular equilibrium. Congenital aniridia is the hallmark of PAX6 gene haploinsufficiency (Chr. 11 p. Read More

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http://dx.doi.org/10.1002/ca.22987DOI Listing
April 2018
10 Reads
1.160 Impact Factor

Twenty-five-gauge sutureless lensectomy in infants with congenital cataract.

J AAPOS 2017 Oct 6;21(5):393-396. Epub 2017 Sep 6.

Department of Ophthalmology, Medical School, Federal University of Rio Grande do Sul and Hospital de Clínicas de Porto Alegre, Porto Alegre RS, Brazil.

Purpose: To evaluate the incidence of intra- and postoperative complications of transconjunctival 25-gauge (25G) sutureless pars plicata lensectomy.

Methods: The medical records of patients <12 months of age with congenital cataracts who underwent 25G sutureless lensectomy were reviewed retrospectively. Patients were evaluated at postoperative days 1, 7, 15, 30, 60, and 90 and every 3 months thereafter. Read More

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https://linkinghub.elsevier.com/retrieve/pii/S10918531163040
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http://dx.doi.org/10.1016/j.jaapos.2017.07.203DOI Listing
October 2017
11 Reads

Iris cysts: A comprehensive review on diagnosis and treatment.

Surv Ophthalmol 2018 May - Jun;63(3):347-364. Epub 2017 Sep 5.

Department of Ophthalmology, National and Kapodistrian University of Athens, 1st University Eye Clinic, G. Gennimatas General Hospital, Athens, Greece.

Iris cysts, both primary and secondary, are a diagnostic and treatment challenge. Primary cysts arise either from the iris pigment epithelium or the iris stroma. Posterior pigment epithelial cysts are subdivided according to their location as central, midzonal, and peripheral. Read More

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http://dx.doi.org/10.1016/j.survophthal.2017.08.009DOI Listing
September 2018
43 Reads

[The analysis of the change of the constitution of the admitted patients with glaucoma].

Zhonghua Yan Ke Za Zhi 2017 Aug;53(8):610-615

Medical Record Department, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing Ophthalmology & Visual Science Key Lab., Beijing 100730, China.

To analysis of the change of the constitution of the admitted patients with glaucoma in Capital Medical University affiliated Beijing Tongren Hospital between 2003-2005(group 2003) and 2013-2015(group 2013). The medical charts information of inpatient with glaucoma were collected by ICD-10 of the disease diagnosis. Statistical analysis was conducted for the change of the proportion of types, gender and age. Read More

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http://dx.doi.org/10.3760/cma.j.issn.0412-4081.2017.08.009DOI Listing
August 2017
1 Read

Congenital Ectropion Uveae with Glaucoma: A Case Report.

J Clin Diagn Res 2017 Jun 1;11(6):ND04-ND05. Epub 2017 Jun 1.

Additional Professor, Department of Ophthalmology, Indira Gandhi Institute of Medical Science, Patna, Bihar, India.

Congenital Ectropion Uveae (CEU) is a rare anomaly characterised by ectropion uveae, iris hypoplasia, iridotrabecular dysgenesis and glaucoma. Hyperplasia of the iris pigment epithelium and its apparent spread over the anterior surface of the iris is supposed to cause the classic ectropion uveae in CEU. Almost all patients develop open angle glaucoma due to angle dysgenesis, so they should be carefully examined periodically for its early detection. Read More

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http://dx.doi.org/10.7860/JCDR/2017/26198.10104DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5535404PMC
June 2017
7 Reads

[Vitiligo occurring on dermal melanocytosis (nevus of Ota) in a dark-skinned patient].

Ann Dermatol Venereol 2017 Nov 17;144(11):712-714. Epub 2017 Jul 17.

Service de dermatologie, CHU, Treichville, Côte d'Ivoire.

Background: Nevus of Ota is a rare disease most frequently found in Asians. It presents clinically as a bluish gray hyperpigmentation of one side of the face. Transformation into melanoma and glaucoma are the main risks. Read More

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http://dx.doi.org/10.1016/j.annder.2017.06.009DOI Listing
November 2017
3 Reads

Congenital aniridia with cataract: case series.

BMC Ophthalmol 2017 Jul 4;17(1):115. Epub 2017 Jul 4.

Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital of Capital Medical University, Beijing Key Laboratory of Ophthalmology and Visual Sciences, Beijing, 100005, China.

Background: This study evaluates patients with congenital aniridia and cataract who underwent phacoemulsification, capsular tension ring placement, and foldable intraocular lens implantation.

Methods: In this prospective case series, 10 patients (17 eyes) underwent cataract surgery via a 3.2 mm clear corneal incision. Read More

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http://dx.doi.org/10.1186/s12886-017-0503-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496261PMC
July 2017
17 Reads

A Case of Bilateral Pigment Dispersion Syndrome Following Many Years of Uninterrupted Treatment With Atropine 1% for Bilateral Congenital Cataracts.

J Glaucoma 2017 Oct;26(10):e225-e228

*Moorfields Eye Hospital, NHS Trust ‡NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, UK †DIBINEM, University of Bologna, Bologna, Italy §Department of Ophthalmology, University Hospital, UANL, Monterrey, México.

Purpose: Describe an unusual case of bilateral pigment dispersion syndrome (PDS) following years of uninterrupted treatment with atropine 1% for bilateral congenital cataracts, speculate on potential mechanisms leading to this condition.

Design: This is a case report.

Case: A 45-year-old white patient on long-term treatment with atropine 1% ointment since his infancy for bilateral congenital cataracts developed PDS with secondary ocular hypertension. Read More

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http://Insights.ovid.com/crossref?an=00061198-201710000-0001
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http://dx.doi.org/10.1097/IJG.0000000000000717DOI Listing
October 2017
4 Reads