Literature DB >> 22165047

Claude Huriez and his syndrome.

Khalid Al Aboud1, Amor Khachemoune.   

Abstract

Claude Huriez (1907-1984) was a well-known French dermatologist. In the 1960s, Huriez and colleagues reported two families from northern France with a rare congenital genodermatosis-later known as Huriez syndrome. This syndrome is characterized by scleroatrophy of the hands and feet, nail hypoplasia, mild palmoplantar keratoderma, and hypohidrosis and is a cancer-prone genodermatosis. This report sheds light on Huriez and the syndrome that bears his name.

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Year:  2011        PMID: 22165047

Source DB:  PubMed          Journal:  Skinmed        ISSN: 1540-9740


  2 in total

1.  A Rare Syndrome Resembling Scleroderma: Huriez Syndrome.

Authors:  Nil Su Çelik; Şirin Yaşar; Sema Aytekin; Pembegül Güneş
Journal:  Skin Appendage Disord       Date:  2017-08-12

2.  Poikiloderma a varied presentation - Huriez syndrome.

Authors:  Priyadarshini Kharge; Carol Fernendes; Vijayeeta Jairath; Madan Mohan; Suresh Chandra
Journal:  Indian Dermatol Online J       Date:  2015 Jan-Feb
  2 in total

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