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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Vydáno v:Front Cell Dev Biol
Hlavní autoři: Wang, Panfeng, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Long, Yuxi, Liu, Mengchu, Li, Yongyu, Li, Jun, Xu, Yan, Zhang, Qingjiong
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2021
Témata:
Cell and Developmental Biology
On-line přístup: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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