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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Bibliographic Details
Main Authors: Fahad Almutawa (Author), Thusanth Thusaringam (Author), Kevin Watters (Author), Tenzin Gayden (Author), Nada Jabado (Author), Denis Sasseville (Author)
Format: Book
Published: Karger Publishers, 2015-08-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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