Leber congenital amaurosis

Leber congenital amaurosis (LCA) is a rare inherited eye disease that appears at birth or in the first few months of life.

2022年10月6日 — Leber congenital amaurosis, also known as LCA, is an eye disorder that is present from birth. Explore symptoms, inheritance, genetics of ...

2022年9月14日 — Leber's congenital amaurosis (LCA) is a rare genetic condition that causes blindness and low vision. It affects the way babies' retinas ...

Leber congenital amaurosis (LCA) is an eye disorder that primarily affects the retina. People with this condition typically have severe visual impairment ...

2018年1月4日 — Leber congenital amaurosis (LCA) is a rare genetic eye disorder. Affected infants are often blind at birth. Other symptoms may include crossed ...

Leber Congenital Amaurosis (LCA). refers to a group of diseases that cause severe vision loss in infancy. The vision loss is due to abnormal function and later ...

由 CH Huang 著作 · 2021 · 被引用 37 次 — Leber's congenital amaurosis (LCA), one of the most severe inherited retinal dystrophies, is typically associated with extremely early onset ...

Leber congenital amaurosis (LCA) is a rare type of inherited eye disorder that causes severe loss of vision at birth, affecting two to three per 100000 ...