Congenital muscular dystrophy with cataracts and intellectual disability

A congenital muscular dystrophy characterized by onset of progressive muscle weakness in early childhood with autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the INPP5K gene (607875) on chromosome 17p13.

Also known as: MDCCAID, muscular dystrophy, congenital, with cataracts and intellectual disability

5 clinical trials for this condition and its sub-types, 0 tagged with Congenital muscular dystrophy with cataracts and intellectual disability itself.