Rett Syndrome (sequence and deletion/duplica- tion analysis of MECP2 gene)(CGC genetics)

Description

Detects mutations and deletions/duplications in the MECP2 gene, which are associated with Rett syndrome, a neurodevelopmental disorder primarily affecting girls.

This lab test includes home sample collection via a provided kit or by a clinician, and you'll receive a comprehensive physical health report with your results.