Poikiloderma a varied presentation - Huriez syndrome

Poikiloderma a varied presentation - Huriez syndrome

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.

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Veröffentlicht in:Indian Dermatology Online Journal 2015-01, Vol.6 (1), p.27-30
Hauptverfasser: Kharge, Priyadarshini, Fernendes, Carol, Jairath, Vijayeeta, Mohan, Madan, Chandra, Suresh
Format: Artikel
Sprache:eng
Schlagworte:
Case Report
Nonfamilial
poikiloderma
squamous cell carcinoma
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Beschreibung
Zusammenfassung: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.
ISSN:2229-5178
2249-5673
DOI:10.4103/2229-5178.148929