CTR9-related neurodevelopmental disorder

Any neurodevelopmental disorder in which the cause of the disease is a variation in the CTR9 gene. This disorder is characterised by varying degrees of intellectual disability, neurodevelopmental delay, hypotonia, fatigability, behavioral abnormalities including autism spectrum disorder, anxiety and aggressive behavior, cardiac anomalies, and mild facial dysmorphism.

0 clinical trials for this condition and its sub-types, 0 tagged with CTR9-related neurodevelopmental disorder itself.