Radio-Tartaglia syndrome

MONDO:0859143

A syndrome that is caused by a variation in the SPEN gene and is characterized by developmental delay/intellectual disability, autism spectrum disorder, anxiety, aggressive behavior, attention deficit disorder, hypotonia, brain and spine anomalies, congenital heart defects, high/narrow palate, facial dysmorphisms, and obesity/increased BMI, especially in females.

Also known as: SPEN-related neurodevelopmental disorder

0 clinical trials for this condition and its sub-types, 0 tagged with Radio-Tartaglia syndrome itself.

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↑ Hereditary disease (18187)

Including sub-types (0) Tagged with Radio-Tartaglia syndrome (0)

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