Cargando…
Differential Diagnosis of Two Chinese Families with Dyschromatoses by Targeted Gene Sequencing
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 types. While clinical and histological presentations...
Autores principales: | Liu, Jia-Wei, Asan, Sun, Jun, Vano-Galvan, Sergio, Liu, Feng-Xia, Wei, Xiu-Xiu, Ma, Dong-Lai |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797540/ https://www.ncbi.nlm.nih.gov/pubmed/26712430 http://dx.doi.org/10.4103/0366-6999.172564 |
Ejemplares similares
-
Use of Targeted Exome Sequencing in Genetic Diagnosis of Chinese Familial Hypercholesterolemia
por: Wu, Wen-Feng, et al.
Publicado: (2014) -
Hair and scalp‐related disorders are a trending topic in dermatology, with a significant increase in number of consultations in the last decade
por: Vano‐Galvan, Sergio
Publicado: (2022) -
Two novel L2HGDH mutations identified in a rare Chinese family with L-2-hydroxyglutaric aciduria
por: Peng, Wei, et al.
Publicado: (2018) -
Technetium and blood extravasation before gammagraphy: a case report
por: Vano-Galvan, Sergio, et al.
Publicado: (2009) -
Two novel SASH1 mutations in Chinese families with dyschromatosis universalis hereditaria
por: Liu, Jia‐Wei, et al.
Publicado: (2021)