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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
rareAn 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.
- Identifiers
- MONDO:0013158 OMIM:613154
- 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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