Congenital Muscular Dystrophy with Cerebellar Involvement

Congenital Muscular Dystrophy with Cerebellar Involvement, also known as cmd with cerebellar involvement, is related to muscular dystrophy-dystroglycanopathy , type c, 14 and autosomal recessive limb-girdle muscular dystrophy type 2w. An important gene associated with Congenital Muscular Dystrophy with Cerebellar Involvement is FKRP (Fukutin Related Protein), and among its related pathways/superpathways are Metabolism of proteins and Diseases of glycosylation. Affiliated tissues include brain and skeletal muscle, and related phenotypes are elevated circulating creatine kinase concentration and congenital muscular dystrophy