Cargando…
Chromosome abnormalities and the genetics of congenital corneal opacification
Congenital corneal opacification (CCO) encompasses a broad spectrum of disorders that have different etiologies, including genetic and environmental. Terminology used in clinical phenotyping is commonly not specific enough to describe separate entities, for example both the terms Peters anomaly and...
Autores principales: | Mataftsi, A., Islam, L., Kelberman, D., Sowden, J.C., Nischal, K.K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123159/ https://www.ncbi.nlm.nih.gov/pubmed/21738392 |
Ejemplares similares
-
Corneal opacification in Sanjad-Sakati syndrome
por: Elhusseiny, Abdelrahman M., et al.
Publicado: (2022) -
Epilation for Trachomatous Trichiasis and the Risk of Corneal Opacification
por: Rajak, Saul N., et al.
Publicado: (2012) -
Enhancement of Corneal Visibility in Optical Coherence Tomography Images with Corneal Opacification
por: Chung, Cheuk Wang, et al.
Publicado: (2016) -
Extracellular matrix changes in corneal opacification vary depending on etiology
por: Módis, László V., et al.
Publicado: (2021) -
Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia
por: Panagiotou, Evangelia S., et al.
Publicado: (2022)