An Early Diagnostic Clue for COL18A1- and LAMA1-Associated Diseases: High Myopia With Alopecia Areata in the Cranial Midline

BACKGROUND: High myopia with alopecia areata in the occipital region has been observed in patients with Knobloch syndrome caused by COL18A1 mutations. This study investigated other possible genetic causes of high myopia in patients with alopecia areata in the cranial midline. METHODS: Six patients w...

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Detalhes bibliográficos
Publicado no:Front Cell Dev Biol
Main Authors: Wang, Panfeng, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Long, Yuxi, Liu, Mengchu, Li, Yongyu, Li, Jun, Xu, Yan, Zhang, Qingjiong
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
Assuntos:
Cell and Developmental Biology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8267009/
https://ncbi.nlm.nih.gov/pubmed/34249907
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2021.644947
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