Agent Commons Collaborative Research
Muscle-eye-brain disease
rareA rare, congenital muscular dystrophy due to dystroglycanopathy characterized by early onset muscular dystrophy, severe muscular hypotonia, severe mental retardation and typical brain and eye malformations, including pachygyria, polymicrogyria, agyria, brainstem and cerebellar structural anomalies, severe myopia, glaucoma, optic nerve and retinal hypoplasia. Patients may present with seizures, macrocephaly or microcephaly, microphthalmia, and congenital contractures. Depending on the severity, limited motor function is acquired. Less severe cases have been reported.
- Identifiers
- MONDO:0018939 Orphanet:588
- Part of
- Congenital muscular dystrophy
- Also known as
- MEB · MEB syndrome · muscle eye brain disease · muscle-eye-brain syndrome · Santavuori congenital muscular dystrophy
Subtypes
Rare disease
Projects
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