Leber congenital amaurosis is an eye disorder that primarily affects the retina, which is the specialized tissue at the back of the eye that detects light ...
Important It is possible that the main title of the report Leber's Congenital Amaurosis is not the name you expected. Please check the synonyms listing to ...
Leber's congenital amaurosis (LCA) is a rare inherited eye disease that appears at birth or in the first few months of life, and affects around 1 in 80,000 of the ...
What is Leber Congenital Amaurosis? Leber Congenital Amaurosis (LCA) is an inherited condition that causes poor vision. Findings commonly first appear after 2-3 ...
Article describes Leber congenital amaurosis, its symptoms, diagnosis, treatment, and areas of research about the disorder.
Leber congenital amaurosis (LCA) is an inherited retinal disease that causes severe visual impairment in infancy or early childhood. Current research on a gene ...
Leber's Congenital Amaurosis (LCA) is a rare genetic disorder in which retinal dysfunction causes vision loss, often from birth. The extent of vision loss varies from ...
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Leber congenital amaurosis is an eye disorder that primarily affects the retina. People with this condition typically have severe visual impairment beginning in infancy.
Leber congenital amaurosis (LCA), a severe dystrophy of the retina, typically becomes evident in the first year of life. Visual function is usually poor and often ...