2007International Journal of DermatologyRequires access

Anhidrotic ectodermal dysplasia with palmoplantar keratoderma: an unusual presentation

Kamaldeep Sandhu, Sanjeev Handa, Amrinder J. Kanwar

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Abstract

Anhidrotic ectodermal dysplasia (AED), or Christ-Siemens-Touraine syndrome, was first described in 1848 by Thurnam. It is characterized by a partial or complete absence of sweat glands, hypotrichosis and hypodontia. The mode of inheritance is predominantly X-linked but an autosomal recessive pattern has also been observed.(2) Palmoplantar keratoderma is classically a component of hidrotic ectodermal dysplasia; however, we report herein two brothers who had classical manifestations of AED along with palmoplantar keratoderma.

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Anhidrotic ectodermal dysplasia (AED), or Christ-Siemens-Touraine syndrome, was first described in 1848 by Thurnam. It is characterized by a partial or complete absence of sweat glands, hypotrichosis and hypodontia. The mode of inheritance is predominantly X-linked but an autosomal recessive pattern has also been observed.(2) Palmoplantar keratoderma is classically a component of hidrotic ectodermal dysplasia; however, we report herein two brothers who had classical manifestations of AED along with palmoplantar keratoderma.

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Available abstract

Anhidrotic ectodermal dysplasia (AED), or Christ-Siemens-Touraine syndrome, was first described in 1848 by Thurnam. It is characterized by a partial or complete absence of sweat glands, hypotrichosis and hypodontia. The mode of inheritance is predominantly X-linked but an autosomal recessive pattern has also been observed.(2) Palmoplantar keratoderma is classically a component of hidrotic ectodermal dysplasia; however, we report herein two brothers who had classical manifestations of AED along with palmoplantar keratoderma.

Key concepts: Ectodermal dysplasia, Hypotrichosis, Palmoplantar keratoderma, Keratoderma, Medicine, Hypodontia, Dermatology, Presentation (obstetrics)

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