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Hereditary palmoplantar keratoderma, Gamborg-Nielsen type
rareHereditary palmoplantar keratoderma, Gamborg-Nielsen type is characterized by the presence of diffuse palmoplantar keratoderma without associated symptoms. The syndrome has been described in multiple families from the northernmost county of Sweden (Norrbotten). The palmoplantar keratoderma found in the Gamborg-Nielsen type disease is milder than that found in Mal de Meleda but more severe than that found in Thost-Unna palmoplantar keratoderma. Transmission is autosomal recessive.
- Identifiers
- MONDO:0009489 OMIM:244850Orphanet:86923
- Part of
- Diffuse palmoplantar keratoderma
- Also known as
- hereditary palmoplantar hyperkeratosis, Gamborg-Nielsen type · palmoplantar keratoderma, Norrbotten recessive type · PPK, Gamborg-Nielsen type · PPKNR
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