GRIN2A-related complex neurodevelopmental disorder

GRIN2A-related complex neurodevelopmental disorder is a group of neurological and neurodevelopmental disorders caused by changes in the GRIN2A gene. These disorders are marked by a broad range of symptoms that can affect a person’s development and neurological function. People with this condition may experience issues with learning and development, as well as challenges in speech and language. The condition is known to affect movement and behavior, and many individuals also cope with epilepsy and neuropsychiatric features.

Common signs and symptoms include developmental delays or intellectual disability, epilepsy, difficulties with speech and language, movement disorders, and neuropsychiatric issues. The symptoms can vary widely among people with this disorder.

GRIN2A-related complex neurodevelopmental disorder is caused by genetic changes in the GRIN2A gene. The variant in this gene affects how the brain develops and functions, which can lead to the range of symptoms seen in people with this condition.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.