Clouston syndrome: First case in Russia

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Abstract

Hidrotic ectodermal dysplasia type 2 (HED2) or Clouston syndrome (OMIM #129500) is a rare autosomal dominant genetic disorder which affects skin and its derivatives, characterized by the major triad of features: nail dystrophy, generalized hypotrichosis, and palmoplantar hyperkeratosis. Here we describe the first case of Clouston syndrome in Russia and the molecular genetic analysis of this case.

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Marakhonov, A. V., Skoblov, M. Y., Galkina, V. A., & Zinchenko, R. A. (2012). Clouston syndrome: First case in Russia. Balkan Journal of Medical Genetics, 15(1), 51–54. https://doi.org/10.2478/v10034-012-0008-9

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