Congenital, Hereditary, and Neonatal Diseases and Abnormalities: News and Research on Eye Diseases, Hereditary

MeSH tree: C16.320.290

Understanding the minutiae of seeing in 3D

So much has to go right as our visual systems develop. One of them is that many thousands of retinal ganglion cells (RGCs) have to relay signals through the eye's optic nerve via delicate projections, or axons, to precise ...

A new device for early diagnosis of degenerative eye disorders

Researchers at an EPFL lab have developed an ophthalmological device that can be used to diagnose some degenerative eye disorders long before the onset of the first symptoms. In early clinical trials, the prototype was shown ...

Researchers home in on a new cause of Stargardt disease

Using a new stem-cell based model made from skin cells, scientists found the first direct evidence that Stargardt-related ABCA4 gene mutations affect a layer of cells in the eye called the retinal pigment epithelium (RPE). ...

High-tech imaging reveals details about rare eye disorder

Using a new imaging technique, researchers from the National Eye Institute have determined that retinal lesions from vitelliform macular dystrophy (VMD) vary by gene mutation. Addressing these differences may be key in designing ...

Trauma of diagnosis stays with eye disease patients

The way in which a patient is told they have serious eye disease can impact their psychological health and ability to cope with their condition in the long-term, according to new research published in the open-access journal ...

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