epidermolytic palmoplantar keratoderma

epidermolytic palmoplantar keratoderma
the most common type of diffuse palmoplantar keratoderma, a genetically heterogeneous, autosomal dominant disorder characterized by epidermolytic hyperkeratosis (q.v.).

Medical dictionary. 2011.

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  • Focal palmoplantar keratoderma with oral mucosal hyperkeratosis — Classification and external resources OMIM 114140 Focal palmoplantar keratoderma with oral mucosal hyperkeratosis (also known as Focal epidermolytic palmoplantar keratoderma, [1] Hereditary painful cal …   Wikipedia

  • diffuse palmoplantar keratoderma — any of several hereditary types of palmoplantar keratoderma; most are autosomal dominant, but a rare type, mal de Meleda, is autosomal recessive. They are usually present in infancy but occasionally do not appear until later. The main… …   Medical dictionary

  • Epidermolytic hyperkeratosis — Classification and external resources ICD 10 Q80.3 OMIM 113800 Diseases …   Wikipedia

  • Keratoderma — Classification and external resources ICD 10 L85.1, L86, Q82.8 …   Wikipedia

  • Vцrner disease — epidermolytic palmoplantar keratoderma …   Medical dictionary

  • List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… …   Wikipedia

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  • Meleda disease — Classification and external resources ICD 10 Q82.8 (ILDS Q82.834) OMIM 248300 Meleda disease (MDM) or mal de Meleda , also called Mljet disease, keratosis palmoplantaris and transgradiens of siemens …   Wikipedia

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