Congenital Central Hypoventilation Syndrome: Sequencing Panel

This test is indicated for: Confirmation of a clinical diagnosis of congenital central hypoventilation syndrome.

Clinical Research Prenatal Carrier

Test Details
Type◦ Molecular
◦ Multi-Gene Panel
GenesASCL1, BDNF, EDN3, GDNF, PHOX2B, RET
Ordering
Test CodeMM244
Turnaround Time12-13 weeks
Preferred SpecimenWhole Blood
Alternate SpecimenIsolated DNA
ShippingShip sample at room temperature with overnight delivery.
Billing
CPT Code◦ 81404
◦ 81406
◦ 81479
 

Laboratory

EGL Genetic Diagnostics, Molecular Genetics Laboratory
2460 Mountain Industrial Boulevard
Tucker
GA 30084
USA

email: eglcs@egl-eurofins.com

Lab Details

 

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