Poikiloderma a varied presentation - Huriez syndrome

• Main Authors: Priyadarshini Kharge (Author), Carol Fernendes (Author), Vijayeeta Jairath (Author), Madan Mohan (Author), Suresh Chandra (Author)
• 格式: 圖書
• 出版: Wolters Kluwer Medknow Publications, 2015-01-01T00:00:00Z.
• 主題: article
• 在線閱讀: Connect to this object online.

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.