Test Background

Mutations in SLC9A6 can cause microcephaly, impaired ocular movement, severe global developmental delay, developmental regression, hypotonia, abnormal movements, and early-onset seizures. It is an X-linked condition. Carrier females may be mildly affected. This laboratory performs Sanger sequencing of the SLC9A6 gene.

Gene(s)

SLC9A6

Vital Information

Test Code:
S0968

Turnaround Time:
2-3 weeks

CPT Code:
81406×1

Billing

Forms and Documents