Dyschromatosis universalis hereditaria: A rare case report

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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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:
Dyschromatosis universalis hereditaria
genodermatosis
dyschromatosis symmetrica hereditaria
Online Access:http://www.jmgims.co.in/article.asp?issn=0971-9903;year=2013;volume=18;issue=2;spage=137;epage=139;aulast=Bisne
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spelling doaj-086ed4595336454a8731f10fede56d012020-11-25T01:00:22ZengWolters Kluwer Medknow PublicationsJournal of Mahatma Gandhi Institute of Medical Sciences0971-99032013-01-0118213713910.4103/0971-9903.117794Dyschromatosis universalis hereditaria: A rare case reportEsha BisneSonia JainV B ShivkumarDyschromatosis 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 overall impression of mottling. Herein, we report this extremely rare case of dyschromatosis universalis hereditaria in a young male with a family history of the same disorder in his younger brother.http://www.jmgims.co.in/article.asp?issn=0971-9903;year=2013;volume=18;issue=2;spage=137;epage=139;aulast=BisneDyschromatosis universalis hereditariagenodermatosisdyschromatosis symmetrica hereditaria
collection DOAJ
language English
format Article
sources DOAJ
author Esha Bisne
Sonia Jain
V B Shivkumar
spellingShingle Esha Bisne
Sonia Jain
V B Shivkumar
Dyschromatosis universalis hereditaria: A rare case report
Journal of Mahatma Gandhi Institute of Medical Sciences
Dyschromatosis universalis hereditaria
genodermatosis
dyschromatosis symmetrica hereditaria
author_facet Esha Bisne
Sonia Jain
V B Shivkumar
author_sort Esha Bisne
title Dyschromatosis universalis hereditaria: A rare case report
title_short Dyschromatosis universalis hereditaria: A rare case report
title_full Dyschromatosis universalis hereditaria: A rare case report
title_fullStr Dyschromatosis universalis hereditaria: A rare case report
title_full_unstemmed Dyschromatosis universalis hereditaria: A rare case report
title_sort dyschromatosis universalis hereditaria: a rare case report
publisher Wolters Kluwer Medknow Publications
series Journal of Mahatma Gandhi Institute of Medical Sciences
issn 0971-9903
publishDate 2013-01-01
description 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 overall impression of mottling. Herein, we report this extremely rare case of dyschromatosis universalis hereditaria in a young male with a family history of the same disorder in his younger brother.
topic Dyschromatosis universalis hereditaria
genodermatosis
dyschromatosis symmetrica hereditaria
url http://www.jmgims.co.in/article.asp?issn=0971-9903;year=2013;volume=18;issue=2;spage=137;epage=139;aulast=Bisne
work_keys_str_mv AT eshabisne dyschromatosisuniversalishereditariaararecasereport
AT soniajain dyschromatosisuniversalishereditariaararecasereport
AT vbshivkumar dyschromatosisuniversalishereditariaararecasereport
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