Pachyonychia congenita: Report of two cases and mutation analysis

Pachyonychia congenita: Report of two cases and mutation analysis

Pachyonychia congenita (PC) comprises a group of rare autosomal dominant genetic disorders that involve ectodermal dysplasia. It is characterized by hypertrophic nail dystrophy, focal palmoplantar keratoderma, follicular keratoses, and oral leukokeratosis. Historically, PC has been subdivided into t...

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Bibliographic Details
Main Authors: Jia-Ming Yeh, Ching-Yuang Huang, Sheau-Chiou Chao
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2012-09-01
Series:Dermatologica Sinica
Subjects:
KRT6A
KRT16
mutation analysis
pachyonychia congenita
Online Access:http://www.sciencedirect.com/science/article/pii/S1027811712000043

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http://www.sciencedirect.com/science/article/pii/S1027811712000043

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