3 results match your criteria patients cleido-cranial

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Multiple, supernumerary retained teeth in the course of cleido-cranial dysplasia. A case report.

Dev Period Med 2015 Oct-Dec;19(4):503-7

Clinical Department of Maxillo-Facial Surgery, Provincial Specialist Hospital in Rzeszów, ul. Chopina 2, 35-005 Rzeszów, Phone 17 866 62 60, 605-547-070, e-mail:

Cleido-cranial dysplasia, often referred to as Scheuthauer-Marie-Sainton syndrome, is an autosomal dominant disorder of the musculo-skeletal system. Patients with cleido-cranial dysplasia are characterized by short stature, frequent varus or valgus hip, kyphoscoliosis, underdevelopment of the scapulas and the sternum, incorrect number of ribs. The most characteristic feature is unilateral or bilateral, partial or total underdevelopment of clavicles. Read More

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Oral manifestation of cleido cranial displasia.

Minerva Stomatol 2012 10;61(10):421-9

Department of Dentistry, Vita Salute University, San Raffele Hospital, Milan, Italy.

Cleidocranial dysplasia (CCD) is a congenital hereditary condition caused by a dominant autosomal mutation. The orthodontic management of CCD patients is often complicated by the manifestations associated with the condition. The aim of this study was to evaluate the oral manifestations of patients suffering from CCD. Read More

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October 2012

[Skull roof reconstruction in infants].

Ned Tijdschr Tandheelkd 1996 Jan;103(1):9-10

Afdeling Mond- en Kaakchirurgie, Academisch Ziekenhuis St. Radboud te Nijmegen, postbus 9101, 6500 HB Nijmegen.

In this article an introduction into craniofacial surgery in children is given based on the case histories of two patients (cleido-cranial dysplasia and cranio-synostosis). Read More

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January 1996
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