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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| Hoofdauteurs: | , , , , |
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| Formaat: | Boek |
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Wolters Kluwer Medknow Publications,
2015-01-01T00:00:00Z.
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Internet
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| Plaatsingsnummer: |
A1234.567 |
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| Kopie 1 | Beschikbaar |