A Case Report of Dyschromatosis Universalis Hereditaria (DUH) with Primary Ovarian Failure (POF)

Autor:	N.S Jayanthi, V. Anandan, W. Afthab Jameela, V. Senthil Kumar, P. Lavanya
Jazyk:	angličtina
Rok vydání:	2016
Předmět:	atp-binding cassette transporters hypothyroidism primary ovarian insufficiency Medicine
Zdroj:	Journal of Clinical and Diagnostic Research, Vol 10, Iss 3, Pp WD01-WD02 (2016)
Druh dokumentu:	article
ISSN:	2249-782X 0973-709X
DOI:	10.7860/JCDR/2016/17525.7368
Popis:	Dyschromatosis Universalis Hereditaria (DUH) belongs to a group of congenital diffuse reticulate pigmentary disorders characterised by both hypo and hyper pigmented macules. It is both hereditary and sporadic. A number of associated cutaneous and systemic diseases have been reported. The recent discovery of the mutation in ATP binding cassette protein, ABCB6 in DUH attempts to explain the reason behind the pigmentary abnormalities and varied associations. We add a new association by reporting a case of DUH with primary ovarian failure (POF) and hypothyroidism.
Databáze:	Directory of Open Access Journals
Externí odkaz:	https://doaj.org/article/a8500033ecbd4146907ae08a77218fcd Zobrazit plný text záznamu View record in DOAJ Plný text ve formátu PDF