Genetic TestsFOXG1 Syndrome

• Test Name: FOXG1 Syndrome
• Test Code: 5572

• “Rett syndrome, congenital variant” (OMIM #: 613454) || Gene: FOXG1 (OMIM #: 164874)

• FORKHEAD BOX G1B
• FOXG1B
• FORKHEAD-LIKE 1
• FKHL1
• ONCOGENE QIN
• BRAIN FACTOR 1; BF1

• Methodology: DNA Sequencing
• Performed: Everyday
• Reported: 4 weeks

• Specimen Collection: Peripheral blood
• Container: Tube with EDTA
• Specimen Volume/Amount: > 5 ml
• Storage/Transport Condition: Refrigerated
• Unacceptable Specimens/Conditions: Serum; Frozen specimens; Hemolyzed specimens; Icterus; Lipemia

• Neurogenetics