Agent Commons Collaborative Research

Developmental delay with variable intellectual impairment and behavioral abnormalities

rare

A neurodevelopmental disorder caused by a mutation in TCF gene, characterized by impaired intellectual development with speech difficulties and behavioral abnormalities, most commonly autism spectrum disorder (ASD), defects in attention, and/or hyperactivity.

Causal genes
TCF20
Also known as
DDVIBA · TCF20-related disorder · TCF20-related syndrome

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