Longitudinal characterization of clinical, developmental, and behavioral phenotypes in 101 children and adults with FOXG1 syndrome

Abstract excerpt

<title>Abstract</title> <p> <bold>Background</bold> FOXG1 syndrome is a severe genetic neurodevelopmental disorder characterized by developmental and intellectual disabilities (DD/ID), postnatal microcephaly, epilepsy, and movement disorder. With the advent of molecular therapies, establishing the natural history of FOXG1 syndrome is critical to enable clinical trial readiness. However, traditional study design...

Topics

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• Developmental Disabilities
• Epilepsy
• Forkhead Transcription Factors
• Intellectual Disability
• Longitudinal Studies
• Movement Disorders
• Neurodevelopmental Disorders
• Syndrome

Identifiers and source

Literature Corpus work

765594d1-6a9d-5942-810d-86e4aebe9f06

DOI

10.21203/rs.3.rs-5582753/v1