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CASE REPORT
Year : 2015  |  Volume : 6  |  Issue : 1  |  Page : 27-30

Poikiloderma a varied presentation - Huriez syndrome


1 Departments of Dermatology, Venereology and Leprosy, Dr. B.R Ambedkar Medical College, Bengaluru, Karnataka, India
2 Department of Pathology, Dr. B.R Ambedkar Medical College, Bengaluru, Karnataka, India

Correspondence Address:
Dr. Vijayeeta Jairath
11-J/2 UH Medical Enclave, Post Graduate Institute of Medical Sciences, Rohtak - 124 001, Haryana
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2229-5178.148929

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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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