Article

The emerging face of FOXG1 Syndrome: a rare, genetically defined neurodevelopmental disorder coming of age in the genomics era.

2024-09-02

Abstract excerpt

<title>Abstract</title> <p><bold>Background and Objectives</bold> FOXG1 Syndrome was first identified in 2005 and has been closely associated with Rett Syndrome. However, with access to genetic testing an increasing number of patients have been identified that do not fulfill Rett Syndrome clinical criteria. Utilizing genetic surveys of large, severe neurodevelopmental disease (NDD) cohorts, we provide the first p...

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Literature Corpus work: dde3c7f0-fdee-53e6-8760-84683f806111
DOI: 10.21203/rs.3.rs-4949811/v1

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