Cargando…
Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract
BACKGROUND: Pediatric cataract is a clinically and genetically heterogeneous disease which is a significant cause of lifelong visual impairment and treatable blindness. Our study aims to investigate the genotype spectrum in a group of Chinese patients with pediatric cataract. METHODS: We enrolled 39...
Autores principales: | Li, Jingyan, Leng, Yunji, Han, Shirui, Yan, Lulu, Lu, Chaoxia, Luo, Yang, Zhang, Xue, Cao, Lihua |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006596/ https://www.ncbi.nlm.nih.gov/pubmed/29914532 http://dx.doi.org/10.1186/s13023-018-0828-0 |
Ejemplares similares
-
Variations in EXD3 caused congenital cataracts in three Chinese families
por: Cao, Lihua, et al.
Publicado: (2022) -
The mutation spectrum in familial versus sporadic congenital cataract based on next-generation sequencing
por: Fan, Fan, et al.
Publicado: (2020) -
Distribution of gene mutations in sporadic congenital cataract in a Han Chinese population
por: Li, Dan, et al.
Publicado: (2016) -
Clinical characteristics of congenital lamellar cataract and myopia in a Chinese family
por: Liu, Qing, et al.
Publicado: (2020) -
Sporadic zonular cataract found by scleral penetration
por: Lee, Chia-Yi, et al.
Publicado: (2021)