muscular dystrophy-dystroglycanopathy congenital muscular dystrophy-dystroglycanopathy type A OMIM:PS236670 A congenital muscular dystrophy-dystroglycanopathy type A characterized by cobblestone lissencephaly, muscle weakness, and brain and eye anomalies that has_material_basis_in autosomal recessive inheritance a defect in alpha-dystroglycan post-translational processing. DOID:0111229 disease_ontology MDDGA ORDO:352687 congenital muscular alpha-dystroglycanopathy with brain and eye anomalies klissencephaly type 2 with muscular and ocular involvement