DIP2C-related developmental disorder with speech delay

A neurodevelopmental disorder caused by variation in the DIP2C gene. This disorder is characterised by developmental delay primarily affect expressive language and speech articulation. Other variable and non-specific phenotypic features include behavioural abnormalities, variable facial anomalies, hypotonia, and structural cardiac anomalies.

0 clinical trials for this condition and its sub-types, 0 tagged with DIP2C-related developmental disorder with speech delay itself.