Description of the disease * EnglishPolish Pobierz sekcję do PDF 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 - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl