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Loricrin keratoderma
rareA diffuse palmoplantar keratoderma, characterized by honeycomb palmoplantar hyperkeratosis associated with pseudoainhum of the fifth digit of the hand, ichthyosis and deafness. Keratoderma hereditarium mutilans with ichthyosis follows an autosomal dominant mode of transmission.
- Identifiers
- MONDO:0011396 OMIM:604117Orphanet:79395
- Causal genes
- LORICRIN
- Part of
- Diffuse palmoplantar keratoderma
- Also known as
- Camisa disease · keratoderma hereditarium mutilans with ichthyosis · keratoderma-ichthyosiform dermatosis-elevated beta-glucuronidase syndrome · Vohwinkel syndrome with ichthyosis
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