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PSTPIP1 Remaining Exons Sequencing

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
PSTPIP1
Disorders:
Clinical Utility:
  • Confirmation of a clinical diagnosis
  • To assist in determining the most appropriate therapy, as the response to specific therapeutic modalities depends on the diagnosis
  • Recurrence risk
  • Prenatal diagnosis
Lab Method:
Capillary Sequencing

ORDERING

Test Code:
2102
Turnaround Time:
5-6 weeks
Preferred Specimen:
2-5 mL Blood - Lavender Top Tube

BILLING

CPT Codes:
81479x1
New York Approved:
No
ABN Required:
Yes
Billing Information:
View Billing Policy
ICD Codes:
  • 279.4: Autoimmune disease, not elsewhere classified
  • 713.7: Other general diseases with articular involvement Code first underlying disease, as: amyloidosis (277.30-277.39), familial Mediterranean fever (277.31) sarcoidosis (135)
  • 277.3: Amyloidosis
* For price inquiries please email zebras@genedx.com

REFERENCES

  1. Wise et al,, (2002) Hum Mol Genet 11:961-969
  2. Shoham et al,, (2003) PNAS 100:13501-13506

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