Indian Journal of Paediatric Dermatology

CASE REPORT
Year
: 2015  |  Volume : 16  |  Issue : 2  |  Page : 102--104

The H syndrome


Sharad Mehta, Vaishali Masatkar, Asit Mittal, Ashok K Khare, Lalit K Gupta 
 Department of Dermatology, Venereology and Leprosy, RNT Medical College, Udaipur, Rajasthan, India

Correspondence Address:
Sharad Mehta
8A, Tulsinagar, Near Sai Baba Temple, Hiranmagri, Sector 5, Udaipur, Rajasthan
India

The H syndrome is a rare autosomal recessive genodermatosis caused by mutations in the nucleoside transporter hENT3. It is characterized by progressive skin sclerosis, hyperpigmentation, and hypertrichosis, along with multiple systemic manifestations including insulin-dependent diabetes mellitus. We report this case for its rarity.


How to cite this article:
Mehta S, Masatkar V, Mittal A, Khare AK, Gupta LK. The H syndrome.Indian J Paediatr Dermatol 2015;16:102-104


How to cite this URL:
Mehta S, Masatkar V, Mittal A, Khare AK, Gupta LK. The H syndrome. Indian J Paediatr Dermatol [serial online] 2015 [cited 2020 Oct 25 ];16:102-104
Available from: https://www.ijpd.in/article.asp?issn=2319-7250;year=2015;volume=16;issue=2;spage=102;epage=104;aulast=Mehta;type=0