Poikiloderma a varied presentation - Huriez syndrome

Abstract

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.

Keywords

• Nonfamilial
• poikiloderma
• squamous cell carcinoma