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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Detalles Bibliográficos
Autores principales: Wang, Panfeng, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Long, Yuxi, Liu, Mengchu, Li, Yongyu, Li, Jun, Xu, Yan, Zhang, Qingjiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267009/
https://www.ncbi.nlm.nih.gov/pubmed/34249907
http://dx.doi.org/10.3389/fcell.2021.644947

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267009/
https://www.ncbi.nlm.nih.gov/pubmed/34249907
http://dx.doi.org/10.3389/fcell.2021.644947

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