Publications by authors named "Farhana Tahseen Taj"

3 Publications

  • Page 1 of 1

Woolly Hair Nevus Type 2: Rare Entity.

Int J Trichology 2019 Jan-Feb;11(1):38-40

Department of Dermatology, Jawaharlal Nehru Medical College, KLE Academy of Higher Education and Research, Belgaum, Karnataka, India.

Woolly hair nevus is a rare non hereditary disorder of scalp characterized by curling and kinking of hair. It can present in childhood or adolescent age. Dermoscopy is a useful noninvasive technique to help in the diagnosis of wolly hair nevus. We report a case of woolly hair nevus associated with linear epidermal nevus.
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http://dx.doi.org/10.4103/ijt.ijt_28_18DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385514PMC
March 2019

Granulosis Rubra Nasi Response to Topical Tacrolimus.

Case Rep Dermatol Med 2017 29;2017:2519814. Epub 2017 Nov 29.

Department of Dermatology, Venereology & Leprosy, Jawaharlal Nehru Medical College and KLE's Dr. Prabhakar Kore Hospital and Medical Research Centre, Belgaum, Karnataka 590 010, India.

Granulosis Rubra Nasi (GRN) is a rare disorder of the eccrine glands. It is clinically characterized by hyperhidrosis of the central part of the face, most commonly on the tip of the nose, followed by appearance of diffuse erythema over the nose, cheeks, chin, and upper lip. It is commonly seen in childhood but it can present in adults. Here we report a case of GRN in an adult patient with very unusual histopathological presentation.
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http://dx.doi.org/10.1155/2017/2519814DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727651PMC
November 2017

Ehlers-Danlos syndrome.

Indian Dermatol Online J 2014 Nov;5(Suppl 1):S68-70

Department of Dermatology, Venereology and leprosy, Dr. Prabhakar Kore Medical Hospital and Research Centre, KLE University, Belgaum, Karnataka, India.

Ehlers-Danlos syndrome (EDS) is a generalized disorder of one element of connective tissue manifesting clinically by fragility and hyperelasticity of the skin and joint laxity. It is a hereditary disorder, the inheritance being usually autosomal dominant with low penetrance. Autosomal recessive and X-linked recessive varieties are also known. First described by Hippocrates in 4(th) century B.C., the various clinical types with variable penetrance have been described lately. The number of cases EDS reported in the literature is very meagre. With the available information only about six publications of classic EDS in siblings had been reported in Indian literature.
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http://dx.doi.org/10.4103/2229-5178.144554DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4252965PMC
November 2014
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