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.
Comprehensive, easy-to-understand information about this condition
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muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
MONDO:0009364
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3
MONDO:0009667
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
MONDO:0013154
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
MONDO:0013157
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
MONDO:0013158
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
MONDO:0013835