Leber’s Congenital Amaurosis
Leber's Congenital Amaurosis (LCA) is a rare, inherited eye disorder that manifests early in life, typically causing severe visual impairment or blindness from birth. LCA is associated with genetic mutations affecting the retina, leading to a range of visual deficits. As research progresses, understanding the genetic basis of LCA holds promise for potential therapies aimed at addressing the underlying causes of this condition.
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