CASE REPORT
Year : 2016 | Volume
: 3 | Issue : 2 | Page : 108--110
Dyschromatosis universalis hereditaria in three siblings
YJ Bhat, I Latief, I Hassan
Postgraduate Department of Dermatology, STD and Leprosy, Government Medical College, Srinagar, University of Kashmir, Jammu Kashmir, India
Correspondence Address:
Dr. Y J Bhat
Assistant Professor, Postgraduate Department of Dermatology, STD and Leprosy, Government Medical College, Srinagar, University of Kashmir, Jammu and Kashmir 190010
India
Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis, which has been reported most often from Japan. The etiology of this disorder is not yet known. DUH is characterized by mixtures of hyperpigmented- and hypopigmented macules all over the body. Skin lesions are usually present in the first years of life. The trunk and extremities are the dominant sites. We report this pigmentary disorder in three siblings, two females and one male. These siblings presented with hypo- and hyperpigmented macules arranged in a reticulate pattern over trunk, dorsal and ventral aspects of legs and arms, and dorsa of both hands and feet. The biopsy findings were also consistent with DUH. Autosomal dominant pattern of inheritance was seen as one of the parents was also affected. There was no systemic involvement.
How to cite this article:
Bhat Y J, Latief I, Hassan I. Dyschromatosis universalis hereditaria in three siblings.Pigment Int 2016;3:108-110
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How to cite this URL:
Bhat Y J, Latief I, Hassan I. Dyschromatosis universalis hereditaria in three siblings. Pigment Int [serial online] 2016 [cited 2022 May 28 ];3:108-110
Available from: https://www.pigmentinternational.com/article.asp?issn=2349-5847;year=2016;volume=3;issue=2;spage=108;epage=110;aulast=Bhat;type=0 |
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