Significados de corneal dystrophy en inglés

One patient had a history of congenital glaucoma with myopia, and one of uveitis with corneal dystrophy.

Schnyder's corneal dystrophy appears to involve the corneal lipid metabolism only and not to be a systemic disease.

Evidence was found for linkage of the gene for Lisch corneal dystrophy to Xp22.3.

Fuchs' endothelial corneal dystrophy (FECD) leads to vision loss and is one of the most common inherited eye diseases.

Methods: We examined at the slit lamp a total of 48 members of a family with an aggregation of Lisch corneal dystrophy.

Avellino dystrophy has not previously been reported to be associated with the R124C mutation, which is usually associated with lattice corneal dystrophy.

All 17 exons of the TGFBI gene were screened for mutations previously associated with lattice corneal dystrophy as well as novel coding region changes.

Methods: A 58-year-old man with a history of recurrent corneal erosions was diagnosed with bilateral anterior basement membrane dystrophy and unilateral lattice corneal dystrophy.

PMID: 11024418 METHODS: We examined at the slit lamp a total of 48 members of a family with an aggregation of Lisch corneal dystrophy.

For the majority of the corneal dystrophies, a phenotype-genotype correlation has not been demonstrated.

Our study suggests that Quercetin is a potential therapeutic for treatment of corneal dystrophies, such as KC.

Conclusions: In cases of suspected TGFBI corneal dystrophies, genetic testing is a useful tool to confirm the clinical diagnosis.

Purpose: To report the utility of genetic testing in the diagnosis and management of patients with suspected corneal dystrophies.

The purpose of this study was to evaluate at the molecular level if Lisch and Meesmann corneal dystrophies are genetically distinct.

PK and ALK were the main techniques of CT and corneal leukoma, bacterial keratitis and corneal dystrophies were the main indications for CT in China.