Disease & disorder
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
MONDO:0009678
Fukuyama type muscular dystrophy (FCMD) is a congenital progressive muscular dystrophy characterized by brain malformation (cobblestone lissencephaly), dystrophic changes in skeletal muscle, severe intellectual deficit, epilepsy and motor impairment.
Outbreak surveillance
Global reported eventsExplore recent public health notices potentially related to muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4. Results are keyword matches, not yet verified disease-to-outbreak relationships.
View muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 on the outbreak map →Advertisement
Drugs being studied
Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.