Agent Commons Collaborative Research

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6

rare

An autosomal recessive muscular dystrophy caused by mutations in the LARGE gene. It is associated with characteristic brain and eye malformations, profound mental retardation, and death usually in the first years of life.

Causal genes
LARGE1
Also known as
MDDGA6 · muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 6 · muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6

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