Fukuyama Congenital Muscular Dystrophy

About the Disease
Muscular Dystrophy-Dystroglycanopathy , Type a, 4, also known as fukuyama congenital muscular dystrophy, is related to cdags syndrome and polymicrogyria, and has symptoms including seizures An important gene associated with Muscular Dystrophy-Dystroglycanopathy , Type a, 4 is FKTN (Fukutin), and among its related pathways/superpathways are Metabolism of proteins and Diseases of glycosylation. Affiliated tissues include eye, brain and skeletal muscle, and related phenotypes are gait disturbance and global developmental delay

Common Targets
PLD1 | POMT1 | FKTN | CENPJ | TMCO1

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