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Hereditary Spastic Paraplegia Related Inborn Errors of Metabolism Panel

New York
Approved


Genes

ABCD1, ARG1, ARSA, BTD, CYP27A1, GALC, GBE1, GCH1, MMACHC, MTHFR, OPA3, PTS, SLC19A3, SPR, TH

Conditions

  • Hereditary Spastic Paraplegia (HSP)

Clinical Utility

  • Molecular confirmation of a clinical diagnosis
  • Identification of at-risk family members
  • Assist with treatment/management decisions

Lab Method

  • Deletion/Duplication Analysis
  • Next-Gen Sequencing

Test Code

944

CPT Codes*

81291x1, 81404x2, 81405x2, 81406x2, 81479x1

ABN Required

No

Turnaround Time**

4 weeks

Preferred Specimen

2-5 mL Blood - Lavender Top Tube

Alternative Specimen

Buccal Swabs

*The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

**Reporting times are typical and begin once the sample(s) are received at the GeneDx laboratory, but could be extended in situations outside GeneDx’s reasonable control.