Leber Congenital Amaurosis D057130

Diseases [C] » Eye Diseases [C11] » Retinal Diseases » Leber Congenital Amaurosis

Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary » Leber Congenital Amaurosis

Description

A rare degenerative inherited eye disease that appears at birth or in the first few months of life that results in a loss of vision. Not to be confused with LEBER HEREDITARY OPTIC NEUROPATHY, the disease is thought to be caused by abnormal development of PHOTORECEPTOR CELLS in the RETINA, or by the extremely premature degeneration of retinal cells.   MeSH

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Phase 3 Indicated Drugs (1)

Phase 1 Indicated Drugs (1)


Organization Involved with Phase 3 Indications (4)

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