Indian Dermatology Online Journal

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

Poikiloderma a varied presentation - Huriez syndrome


Priyadarshini Kharge1, Carol Fernendes1, Vijayeeta Jairath1, Madan Mohan1, Suresh Chandra2 
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

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.


How to cite this article:
Kharge P, Fernendes C, Jairath V, Mohan M, Chandra S. Poikiloderma a varied presentation - Huriez syndrome.Indian Dermatol Online J 2015;6:27-30


How to cite this URL:
Kharge P, Fernendes C, Jairath V, Mohan M, Chandra S. Poikiloderma a varied presentation - Huriez syndrome. Indian Dermatol Online J [serial online] 2015 [cited 2022 Jan 17 ];6:27-30
Available from: https://www.idoj.in/article.asp?issn=2229-5178;year=2015;volume=6;issue=1;spage=27;epage=30;aulast=Kharge;type=0