nonepidermolytic palmoplantar keratoderma

nonepidermolytic palmoplantar keratoderma
a rare autosomal dominant type of diffuse palmoplantar keratoderma in which there is hyperkeratosis without epidermolysis and characteristic focal oral, genital, and follicular lesions. Called also Unna-Thost syndrome.

Medical dictionary. 2011.

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  • Diffuse nonepidermolytic palmoplantar keratoderma — Classification and external resources ICD 10 Q82.8 (ILDS Q82.836) OMIM 600962 Diffuse nonepidermolytic palmoplantar keratoderma (also known as Diffuse orthohyperkeratotic keratoderma, Hereditary palmoplantar keratoder …   Wikipedia

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  • 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

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

  • Unna-Thost syndrome — nonepidermolytic 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

  • 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

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

  • Connective tissue disease — Classification and external resources MeSH D003240 A connective tissue disease is any disease that has the connective tissues of the body as a target of pathology. Connective tissue is any type of biological tissue with an extensive extracellular …   Wikipedia

  • Naegeli–Franceschetti–Jadassohn syndrome — Classification and external resources OMIM 161000 DiseasesDB 29767 eMedicine …   Wikipedia

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