Open AccessPoikiloderma a varied presentation - Huriez syndrome
Author(s) -
Priyadarshini Kharge,
Carol Fernendes,
Vijayeeta Jairath,
Madan Mohan,
Suresh Chandra
Publication year - 2015
Publication title -
indian dermatology online journal
Language(s) - English
Resource type - Journals
eISSN - 2249-5673
pISSN - 2229-5178
DOI - 10.4103/2229-5178.148929
Subject(s) - genodermatosis , medicine , poikiloderma , presentation (obstetrics) , dermatology , keratoderma , palmoplantar keratoderma , surgery , hyperkeratosis , genetics , gene , biology
Huriez syndrome is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma (PPK) and hypoplastic nails. We report the case of a 25 year old male, with nonfamilial Huriez syndrome.