Zobrazeno 1 - 10
of 169
pro vyhledávání: '"dyschromatosis universalis hereditaria"'
Autor:
Veena
Publikováno v:
Pigment International, Vol 9, Iss 1, Pp 55-58 (2022)
Dyschromatosis Universalis hereditaria is a rare pigmentary disorder presenting with dyschromia of skin involving trunk and extremities arranged in mottled manner lesions, usually present in the first few years of life. Herein, we report this extreme
Externí odkaz:
https://doaj.org/article/3cfef83b7918404aabdbe9198c4c2fb8
Autor:
Lu Cao, Ruixue Zhang, Liang Yong, Shirui Chen, Hui Zhang, Weiwei Chen, Qiongqiong Xu, Huiyao Ge, Yiwen Mao, Qi Zhen, Yafen Yu, Xia Hu, Liangdan Sun
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-8 (2021)
Abstract Background Dyschromatosis universalis hereditaria (DUH) is a pigmentary dermatosis characterized by generalized mottled macules with hypopigmention and hyperpigmention. ABCB6 and SASH1 are recently reported pathogenic genes related to DUH, a
Externí odkaz:
https://doaj.org/article/a4b9f9a6723749759c070dd51d7d7d14
Publikováno v:
JAAD Case Reports, Vol 11, Iss , Pp 23-25 (2021)
Externí odkaz:
https://doaj.org/article/7e352eaee57e4b4cad50bc9093d3f64e
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis characterized by mottled hyperpigmented and hypopigmented macules. SASH1 and ABCB6 have been identified as the causative genes for this disorder. We performed whole exome sequencin
Externí odkaz:
https://doaj.org/article/d1e2645286e54f6eb3aa181378d2563a
Autor:
Yiming Li, MD, PhD, Li Li, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 4, Iss 1, Pp 104-106 (2018)
Externí odkaz:
https://doaj.org/article/8f017b18c36744958a0d8b7fbef62b86
Autor:
Kikkeri Narayanshetty Naveen, Sharatchandra B Athaniker, Spandana P Hegde, Rahul Shetty, Hanumanthayya Radha, Sadashivappa Sangam Parinitha
Publikováno v:
Indian Dermatology Online Journal, Vol 7, Iss 2, Pp 99-102 (2016)
Dowling–Degos disease (DDD) is a rare autosomal dominant condition characterized by multiple, small, round pigmented macules usually arranged in reticular pattern, chiefly distributed in axillae and groins. Here we are reporting three atypical case
Externí odkaz:
https://doaj.org/article/7e140de777ea46049e68ed00282e171a
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 1, Pp 33-38 (2016)
Background: The dyschromatoses are a group of disorders characterized by simultaneous hyperpigmented macules together with hypopigmented macules. Dyschromatosis universalis hereditaria (DUH) and dyschromatosis symmetrica hereditaria are two major typ
Externí odkaz:
https://doaj.org/article/60e6a8563b9d4bc9be996450e135982b
Publikováno v:
Case Reports in Dermatology, Vol 7, Iss 1, Pp 51-55 (2015)
Dyschromatosis universalis hereditaria (DUH) is a rare autosomal dominant inherited dermatosis which usually appears during childhood and is characterized by dyspigmentation, with both hypopigmented and hyperpigmented macules. We report a case of DUH
Externí odkaz:
https://doaj.org/article/45a349d2d22640dc90310077f9759fa2
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 18, Iss 1, Pp 43-45 (2017)
Dyschromatosis universalis hereditaria (DUH) is a rare genodermatoses characterized by hyperpigmented and hypopigmented macules inherited most commonly in autosomal dominant manner. We hereby report a case of DUH in an adolescent male with palmo-plan
Externí odkaz:
https://doaj.org/article/0deb1c050b3b493b8e8cc5c0c88c7733
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 2, Pp 105-109 (2015)
Dyschromatosis universalis hereditaria (DUH) is a rare, autosomal dominant genodermatosis with a peculiar reticulate pigmentary change, consisting of hyperpigmented macules mingled with hypopigmented lesions to give an overall impression of mottling.
Externí odkaz:
https://doaj.org/article/066892bffcb9413bab0c24f021bf2c4c