FOXG1 Sequencing

Test Background

The congenital variant of Rett syndrome is a severe neurodevelopmental disorder with features of classic Rett syndrome (see Rett syndrome description), but earlier onset in the first months of life. This laboratory performs Sanger sequencing of the FOXG1 gene.

Disorder(s)

Rett syndrome

Gene(s)

FOXG1

About Claritas

Claritas Genomics serves children affected with complex genetic disorders by providing timely and accurate results, resolving families’ long search for answers. By combining clinical expertise of the world’s best pediatric specialists with innovative platform solutions, Claritas is working to improve patient care and enable new discoveries. We are committed to the highest quality and accessibility of information and our interpretive services and unique approach to reporting set the standard for reliably and clearly communicating genetic information.

Now is the time to integrate genomics into clinical practice to inform, guide and improve medical treatment for kids around the world.