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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Bibliographic Details
Main Authors: Priyadarshini Kharge (Author), Carol Fernendes (Author), Vijayeeta Jairath (Author), Madan Mohan (Author), Suresh Chandra (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2015-01-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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