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HADHB Gene Sequencing

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
HADHB
Disorders:
Clinical Utility:
  • Diagnostic confirmation
  • Carrier testing
  • Prenatal diagnosis in at-risk pregnancies
Lab Method:
Capillary Sequencing

ORDERING

Test Code:
272
Turnaround Time:
6-8 weeks
Preferred Specimen:
2-5 mL Blood - Lavender Top Tube

BILLING

CPT Codes:
81406x1
New York Approved:
No
ABN Required:
Yes
Billing Information:
View Billing Policy
ICD Codes:
  • 277.85: Disorders of fatty acid oxidation, Carnitine palmitoyltransferase deficiencies, Glutaric aciduria type II, Long chain 3-hydroxyacyl CoA dehydrogenase deficiency (LCHAD), Long chain/very long chain acyl CoA dehydrogenase deficiency, Medium chain acyl CoA dehydrogenase deficiency (MCAD), Short chain acyl CoA dehydrogenase deficiency (SCAD)
* For price inquiries please email zebras@genedx.com

REFERENCES

  1. Tyni, T and Pihko, H. (1999) Acta Paediatr 88:237-245
  2. Hintz, S. R., et al. (2002) Mol Genet Metab 75:120-127
  3. den Boer MEJ, et al. (2002) Pediatrics 109:99-104
  4. Ibdah, J.A., et al. (1999) N Engl J Med 340:1723-1731
  5. Das, A.M. et al., (2006) Clin Chem 52:530-534

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