Document Detail
Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of dohi): First report from Iran
Abstract/OtherAbstract :
Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant genodermatosis, presenting in infancy or early childhood with areas of hyperpigmentation on dorsa of hands and feet. DSH has been reported mainly from Japan and only limited cases have been reported from other countries. This is the first report of an Iranian patient with this rare type of acropigmentation. Our patient′s family history was striking with the same disorder in her grandmother, mother, uncle and her two older sisters which reveal an autosomal dominant pattern of inheritance.
Authors :
Barzegari Massoumeh, Kiavash Katrin
Contributors :
Publication Detail :
Publisher :  Medknow Publications     Type :  -     Format :  -    
Date Detail :
Subject :
<i>Dyschromatosis symmetrica hereditaria, reticulate acropigmentation of Dohi, acropgmentation of kitamura </i>
Coverage :
Relation :
Source :
Indian Journal of Dermatology
Copyright Information :
Other Details :
Languages :  EN    
Export Citation :
APA/MLA Format     Download EndNote     Download BibTex

Previous Document:  Hypertrophic lichen planus as a presenting feature of human immunodeficiency virus infection
Next Document:  Marjolin ulcer with multifocal origin