Case report: Familial foveal retinoschisis caused by CRB1 gene mutation in a family with recessive inheritance

X-linked retinoschisis is more common in male children and rare in females. Clinically, male patients mainly present with early onset visual impairment or vision loss, and retinal retinoschisis due to division of the inner retina. We report a long-term observation of a female patient with familial f...

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Detalles Bibliográficos
Autores principales: Liu, Shu, Ren, Yue, Wang, Di, Xiao, Dan, Li, Zhuang, Xu, Dan, Sun, Yan, Wang, Zhuoshi, Pang, Jijing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10451074/
https://www.ncbi.nlm.nih.gov/pubmed/37636578
http://dx.doi.org/10.3389/fmed.2023.1220075

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10451074/
https://www.ncbi.nlm.nih.gov/pubmed/37636578
http://dx.doi.org/10.3389/fmed.2023.1220075

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