Dyschromatosis universalis hereditaria: A rare case report

Dyschromatosis universalis hereditaria is an autosomal dominant disorder but may be recessive or sporadically inherited disorder, infrequently occurring genodermatosis with peculiar pigmentary changes, consisting of varying sized, intermingled hyperpigmented and hypopigmented macules that give an ov...

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Bibliographic Details
Main Authors: Esha Bisne, Sonia Jain, V B Shivkumar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2013-01-01
Series:Journal of Mahatma Gandhi Institute of Medical Sciences
Subjects:
Online Access:http://www.jmgims.co.in/article.asp?issn=0971-9903;year=2013;volume=18;issue=2;spage=137;epage=139;aulast=Bisne