Diffuse nonepidermolytic palmoplantar keratoderma

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 keratoderma," "Keratosis extremitatum progrediens," "Keratosis palmoplantaris diffusa circumscripta," "Tylosis," "Unna–Thost disease", and "Unna–Thost keratoderma"^[1]) is inherited as an autosomal dominant condition and is present from infancy, characterized by a well-demarcated, symmetric, often "waxy" keratoderma involving the whole of the palms and soles.^{[2]:506-8[3]:213}

See also

• Palmoplantar keratoderma
• Keratoderma
• Skin lesion
• List of cutaneous conditions

References

1. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. pp. 778. ISBN 1-4160-2999-0. 
2. ^ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0071380760.
3. ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0721629210.

This cutaneous condition article is a stub. You can help Wikipedia by expanding it.v · Categories: Cutaneous condition stubs Palmoplantar keratodermas Wikimedia Foundation. 2010. Игры ⚽ Нужно решить контрольную? Naxos syndrome Diffuse noxious inhibitory control Look at other dictionaries: 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 Palmoplantar keratoderma — Classification and external resources A picture of a 40 y/o Caucasian female with only the soles of the feet affected. The amputation was prior to this admission ICD 10 L …   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 Keratoderma — Classification and external resources ICD 10 L85.1, L86, Q82.8 …   Wikipedia 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 Confluent and reticulated papillomatosis — of Gougerot and Carteaud Classification and external resources ICD 10 L83 OMIM 167900 Confluent and reticulated papillomatosis of Gougerot and Carteaud (also known as Confluent and reticulated papillomatosis, Familial cutaneou …   Wikipedia 18+ © Academic, 2000-2024 Contact us: Technical Support, Advertising Dictionaries export, created on PHP, Joomla, Drupal, WordPress, MODx. Mark and share Search through all dictionaries Translate… Search Internet Share the article and excerpts Direct link … Do a right-click on the link above and select “Copy Link”