Congenital muscular dystrophy with intellectual disability

Også kjent som: Congenital MD with intellectual disability
Engelsk navn: Congenital muscular dystrophy with intellectual disability
Engelske synonym: CMD with intellectual disability,CMD-MR


A rare, genetic, congenital muscular dystrophy due to dystroglycanopathy disorder characterized by a wide phenotypic spectrum which includes hypotonia and muscular weakness present at birth or early infancy and delayed or arrested motor development, associated with mild to severe intellectual disability and variable brain abnormalities on neuroimaging studies. Feeding difficulties, joint and spinal deformities, respiratory insufficiency, and ocular anomalies (e.g. strabismus, retinal dystrophy, oculomotor apraxia) may be associated. Decreased or absent alpha-dystroglycan on immunohistochemical muscle staining and elevated serum creatine kinase are observed.

Fra Orphanet

ORPHA: 370968
Klassifiseringsnivå: Disorder
ICD-10: G71.2

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