Muscle-eye-brain disease

Orpha code: 588OMIM code: 615350

Definicja

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
Klasyfikacja

Malformation syndrome

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

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl