FOXG1 Sequencing

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.

Forms & Docs

Ordering

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Test Code
S0823

Turn Around Time
2-3 weeks

Billing

CPT Code
81404×1

Ordering Guidance

To be ordered if methylation and deletion analysis for Angelman syndrome was normal and/or if MECP2 sequencing and deletion/duplication for Rett syndrome was normal

If there are questions regarding this test, please contact Client Services at 617-553-5880 or clientservices@claritasgenomics.com

Details

Genes Covered
FOXG1

Methods
Sanger