Results 131 to 136 of about 401 (136)

A RARE CASE REPORT OF DYSCHROMATOSIS UNIVERSALIS HEREDITARIA

INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH
Dyschromatosis universalis hereditaria (DUH) is a rare genetic skin condition that involves a mixture of hyperpigmented and hypopigmented macules with mottled pigmentation. Lesions usually start on the limbs and extend to the trunk over time. Cases in the Indian population are extremely uncommon, with the majority of recorded cases emanating from Japan.
Akshata Yadav. S, Rajashekar T.S, Sureshkumar. K   +2 more
openaire   +1 more source

Dyschromatosis Universalis Hereditaria

2014
Pirasath Selladurai, KT Sundaresan, N Tamilvannan   +2 more
openaire   +1 more source

Novel missense mutations of ABCB6 in two chinese families with dyschromatosis universalis hereditaria

Journal of Dermatological Science, 2014
Chaoxia Lu, Yaping Liu, Donglai Ma
exaly  

Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation

American Journal of Medical Genetics, Part A, 2004
Stefan Mundlos
exaly  

Abrupt onset of dyschromatosis universalis hereditaria with macromelanosomes

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2015
Yue Shi, Cheng Tan
openaire   +1 more source

Dyschromatosis universalis hereditaria with sensorineural hearing loss

Egyptian Journal of Dermatology and Venereology, 2016
openaire   +1 more source