Hypomyelination-congenital cataract syndrome (original) (raw)

Hypomyelination-congenital cataract syndrome is a rare autosomal recessive hereditary disorder that affects the brain's white matter and is characterized by congenital cataract (or cataracts that begin in the first two months of life), psychomotor development delays, and moderate intellectual disabilities. It is a type of leukoencephalopathy.