Christ-Siemens-Touraine Syndrome: A Case Report and Review of the Literature

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Christ Siemens Touraine syndrome: a case report

BACKGROUND The ectodermal dysplasias are a large and complex group of diseases. CASE PRESENTATION This article presents a case in a 37 years old female patient, referred to the dental clinic for impairment patients maintained by the University of Pernambuco. She presented typical characteristics of Christ Siemens Touraine syndrome such as alterations of the inferior members, a great number of...

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Christ-Siemens-Touraine Syndrome: A Case Report and Review of the Literature

ECTODERMAL DYSPLASIA IS A RARE DISORDER WITH DEFECTS IN TWO OR MORE OF THE FOLLOWING STRUCTURES: the teeth and the skin and its appendages including hair, nails, eccrine, and sebaceous glands. Anhidrotic ectodermal dysplasia is the most common type of disease. This rare disorder, also known as Christ-Siemens-Touraine syndrome, manifests as a triad of hypotrichosis, asteatosis, and anhidrosis. I...

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Christ–Siemens–Touraine syndrome with palmoplantar keratoderma: A rare association

Christ-Siemens-Touraine syndrome is a form of anhidrotic ectodermal dysplasia (ED) characterized by triad of hypodontia, hypotrichosis, and hypohidrosis. Palmoplantar keratoderma is a characteristic feature of hidrotic forms of ED. Till date, only two cases have been reported of Christ-Siemens-Touraine syndrome with palmoplantar keratoderma; here we report a similar case emphasizing this rare a...

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McCune-Albright Syndrome: A Case Report and Literature Review

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Touraine-Soulente-Golé Syndrome (TSG) or pachydermoperiostosis is a rare disorder characterized by pachydermia, periostosis & digital clubbing. Herein, we report a case of a 27 year old male, with the looks of a 47 year old. He presented with excessive wrinkling on his face since past 8 years. TSG syndrome was suspected and examined by histopathological, endocrinological and radiological studie...

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ژورنال

عنوان ژورنال: Case Reports in Dentistry

سال: 2012

ISSN: 2090-6447,2090-6455

DOI: 10.1155/2012/586418