Pachyonychia Congenita (K16) with Unusual Features and Good Response to Acitretin

BACKGROUND: Pachyonychia congenita (PC) is a rare autosomal dominant disease whose main clinical features include hypertrophic onychodystrophy and palmoplantar keratoderma. The new classification is based on genetic variants with mutations in keratin KRT6A, KRT6B, KRT6C, KRT16, KRT17, and an unknown...

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Detalles Bibliográficos
Autores principales: Almutawa, Fahad, Thusaringam, Thusanth, Watters, Kevin, Gayden, Tenzin, Jabado, Nada, Sasseville, Denis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2015
Materias:
Published online: August, 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592507/
https://www.ncbi.nlm.nih.gov/pubmed/26464567
http://dx.doi.org/10.1159/000438920

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592507/
https://www.ncbi.nlm.nih.gov/pubmed/26464567
http://dx.doi.org/10.1159/000438920

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