Muscle-eye-brain disease

Orpha code: 588OMIM code: 615350

Definition

A 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.

Disease data
Classification

Malformation syndrome

Synonyms
MEB syndrome
Wrodzona dystrofia mięśniowa Santavuori
Zespół MEB
Zespół mięsień-oko-mózg
Muscle-eye-brain syndrome
Santavuori congenital muscular dystrophy
ORPHA code
588
OMIM code
615350
ICD10 code
G71.0
ICD11 code
-

No additional description.

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