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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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
Karger Publishers,
2015-08-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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