Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.
Ontology highlight
ABSTRACT: Cataracts are the principal cause of treatable blindness worldwide. Inherited congenital cataract (CC) shows all types of inheritance patterns in a syndromic and nonsyndromic form. There are more than 100 genes associated with cataract with a predominance of autosomal dominant inheritance. A cataract is defined as an opacity of the lens producing a variation of the refractive index of the lens. This variation derives from modifications in the lens structure resulting in light scattering, frequently a consequence of a significant concentration of high-molecular-weight protein aggregates. The aim of this review is to introduce a guide to identify the gene involved in inherited CC. Due to the manifold clinical and genetic heterogeneity, we discarded the cataract phenotype as a cardinal sign;
SUBMITTER: Messina-Baas O
PROVIDER: S-EPMC5465711 | biostudies-literature | 2017 Mar
REPOSITORIES: biostudies-literature
ACCESS DATA