Cargando…
Rare eye diseases in India: A concise review of genes and genetics
Rare eye diseases (REDs) are mostly progressive and are the leading cause of irreversible blindness. The disease onset can vary from early childhood to late adulthood. A high rate of consanguinity contributes to India’s predisposition to RED. Most gene variations causing REDs are monogenic and, in s...
Autores principales: | Jeyabalan, Nallathambi, Ghosh, Anuprita, Mathias, Grace P., Ghosh, Arkasubhra |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9426079/ https://www.ncbi.nlm.nih.gov/pubmed/35791102 http://dx.doi.org/10.4103/ijo.IJO_322_22 |
Ejemplares similares
-
Autophagy in dry eye disease: Therapeutic implications of autophagy modulators on the ocular surface
por: Jeyabalan, Nallathambi, et al.
Publicado: (2023) -
Genetic and genomic perspective to understand the molecular pathogenesis of keratoconus
por: Jeyabalan, Nallathambi, et al.
Publicado: (2013) -
Retinoblastoma genetics screening and clinical management
por: Gupta, Himika, et al.
Publicado: (2021) -
Two novel missense substitutions in the VSX1 gene: clinical and genetic analysis of families with Keratoconus from India
por: Shetty, Rohit, et al.
Publicado: (2015) -
Chloroquine Protects Human Corneal Epithelial Cells from Desiccation Stress Induced Inflammation without Altering the Autophagy Flux
por: Shivakumar, Shivapriya, et al.
Publicado: (2018)