Granular corneal dystrophy, type II (CGD2; Avellino corneal dystrophy) is the most common corneal dystrophy among Koreans, but its pathophysiology is still poorly understood. Many reports showed ...

Patient with granular corneal dystrophy immediately following epithelial debridement prior to PTK. Source: William B. Trattler, MD 3 and 4. During and after PTK for granular dystrophy.

Granular corneal dystrophy type 1 (GCD1) is a progressive genetic condition that develops from an early age and leads to corneal erosion, pain and decreased vision.

Granular corneal dystrophy (GCD) is characterized by the deposition of small, discrete, sharply demarcated, greyish white opacities in the anterior stroma.

Granular corneal dystrophy presents with clear zones between the opacities, which are absent in macular dystrophy. Based upon the clinical appearance and optical coherence tomography ...

A corneal dystrophy is a condition in which one or more parts of the cornea lose their normal clarity because of a buildup of cloudy material. There are over 20 corneal dystrophies that affect all ...

Fuchs’ corneal dystrophy is a genetic eye disease. In the early stages, it causes bumps called guttae to form on cells in your cornea. In the late stages, it can make your cornea swell.

About BGI's Granular Corneal Dystrophy SNP Detection Kit. BGI Genomics' Granular GCD SNP Detection Kit has obtained CE-IVDD approval.

Granular Corneal Dystrophy SNP Detection Kit. Credit. BGI Genomics. Usage Restrictions. Journalists may use in their content. License. Original content.

Woman who received cornea transplant celebrates seeing her children play after support from Waiting for Life organ donor program. Published: Apr. 17, 2013, 5:14 p.m. By .

Corneal dystrophies, including granular corneal dystrophy, have distinct clinical features that are recognized on slit lamp examination.