Leber Congenital Amaurosis
Body function: Eyes
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Leber congenital amaurosis, or congenital night blindness, is a genetic disorder caused by a mutation in the RPE65 gene. It causes retina degeneration, leading to loss of night vision and, ultimately, total blindness. It is inherited in the autosomal recessive fashion, meaning both parents must be carriers for a litter to risk developing the condition.
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