Neurodevelopmental disorder with cerebellar atrophy and with or without seizures

An an autosomal recessive disorder characterized by intellectual disability associated with ataxia, in which the cause of the disease is a variation in the BRAT1 gene.

Also known as: NEDCAS, neurodevelopmental disorder with cerebellar atrophy and with or without seizures

0 clinical trials for this condition and its sub-types, 0 tagged with Neurodevelopmental disorder with cerebellar atrophy and with or without seizures itself.