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Other links at Retina > Leber's Congenital Amaurosis
Description of the genes responsible for causing LCA, including information about genetic testing and differential diagnoses.
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Forwarding to NCBI Bookshelf :
Leber Congenital Amaurosis
Funded by the NIH • Developed at the University of Washington, Seattle
Richard G Weleber, MD, FABMG, FACMG
Peter J Francis, FRCOphth, PhD
Karmen M Trzupek, MS, CGC
amaurosis (LCA), a severe dystrophy of the retina, typically
waiting for hand_moderation
Dr. Edwin Stone delivers a presentation on the disease, its genotype, and current genetic breakthroughs.
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Ophthalmology Case Reports and Grand Rounds from the University of Iowa Department of Ophthalmology & Visual Sciences
Genetic Testing for Leber congenital amaurosis
Presented at the New England Ophthalmological Society
, 200 Hawkins Dr., Iowa City, IA 52242-1091. Last updated: 04-08-2005
To Access Navigation, see our
The University of Iowa Department of Ophthalmology and Visual
Sciences has a long history of
Information about the condition (along with background about heredity and eye function), resources for families, and solicitation for donations to fund research.
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leber's leber's leber's leber's leber's leber's leber's The Foundation for Retinal Research - Walking With A Vision. More than six million people in the United States alone are blind or visually impaired from degenerative retinal diseases. These groups of diseases, which include Macular Degeneration, Retinitis Pigmentosa, Sargardt's Disease and Leber's Congenital Amaurosis, affect the retina, where light is converted- into signals to the brain.
FOUNDATION FOR RETINAL RESEARCH
The Foundation for Retinal Research and
are proud to announce the dates for
2010 LCA Family Conference
When: Friday, July 30 th August 1, 2010
Follow the Link below to Register:
Hotel: Inn at Penn, Philadelphia, PA
follow the link below for reservations
The