Childhood cone–rod dystrophy with macular cyst formation in ABCA4 mutation identified by serial spectral-domain optical coherence tomography

Cone–rod dystrophy (CORD) is a type of progressive hereditary retinal dystrophies that causes cone predominant photoreceptor degeneration characterized by wide genotypic and phenotypic heterogeneity. Macular cyst (MC) occurs very infrequently in the pediatric age group and has rarely been described...

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Detalles Bibliográficos
Autores principales: Leung, Kai Ching Peter, Ko, Tak Chuen Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493982/
https://www.ncbi.nlm.nih.gov/pubmed/34703750
http://dx.doi.org/10.4103/tjo.tjo_54_20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493982/
https://www.ncbi.nlm.nih.gov/pubmed/34703750
http://dx.doi.org/10.4103/tjo.tjo_54_20

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