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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.

Child Wearing Glasses Without Lenses

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