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.

Also known as: FCMD, Fukuyama Type Congenital Muscular Dystrophy, Fukuyama congenital muscular dystrophy, MDDGA4, Walker-Warburg syndrome or muscle-eye-brain disease, FKTN-related, muscle-eye-brain-FKTN related, muscular dystrophy-dystroglycanopathy (congenital with Brain and eye anomalies) type A, 4, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4

5 clinical trials for this condition and its sub-types, 0 tagged with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 itself.

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↑ Myopathy caused by variation in FKTN (2) ↑ Muscular dystrophy-dystroglycanopathy, type A (1) ↑ Muscle-eye-brain disease (0)

Including sub-types (5) Tagged with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 (0)

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