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Printable Test Catalog - OU Medicine

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SPECIMEN REQUIRED: Whole blood at room temperature<br />

TUBE OR CONTAINER: Lavender (EDTA) or Yellow (ACD)<br />

SPECIMEN VOLUME: 5 mL<br />

MINIMUM VOLUME: 1 mL<br />

TEST AVAILABILITY: Daily<br />

TURNAR<strong>OU</strong>ND TIME: 4 weeks<br />

OTHER NAMES: Faciogenital Dysplasia, Faciodigitogenital<br />

Syndrome, Faciogenital Dysplasia with Attention<br />

Deficit-Hyperactivity Disorder, FGD1 Gene<br />

Sequencing<br />

METHODOLOGY: Polymerase chain reaction (PCR)<br />

CPT: 83891; 83894; 83898 x 18; 83904 x 36; 83909 X 36; 83912<br />

[FGFR] CRANIOSYNOSTOSIS/FGFR<br />

SPECIMEN REQUIRED: Whole blood at room temperature<br />

TUBE OR CONTAINER: Lavender (EDTA)<br />

SPECIMEN VOLUME: 5 mL<br />

MINIMUM VOLUME: 2 mL<br />

TEST INCLUDES: FGFR 1, 2 and 3<br />

TEST AVAILABILITY: Daily<br />

TURNAR<strong>OU</strong>ND TIME: 3 weeks<br />

METHODOLOGY: PCR amplification and DNA sequencing of exon 7 and<br />

9 (IIIa and IIIc) of the FGFR2 gene, and point<br />

mutation testing of the FGFR1 and FGFR3 genes<br />

CPT: 83890; 83892 x 6; 83894 x 3; 83898 x 6; 83904 x 6; 83912<br />

[FGFR2SEQ] CRANIOSYNOSTOSIS/FGFR2 GENE<br />

SPECIMEN REQUIRED: Whole blood at room temperature<br />

TUBE OR CONTAINER: Lavender (EDTA)<br />

SPECIMEN VOLUME: 5 mL<br />

MINIMUM VOLUME: 2 mL<br />

TEST AVAILABILITY: Daily<br />

TURNAR<strong>OU</strong>ND TIME: 4-6 weeks<br />

METHODOLOGY: PCR amplification and DNA sequencing of exon 7 and<br />

9 (IIIa and IIIc) of the FGFR2 gene<br />

CPT: 83890; 83894 x 2; 83898 x 23; 83904 x 48; 83909; 83912<br />

[FHAB] Complement Factor H<br />

SPECIMEN REQUIRED: Frozen serum<br />

TUBE OR CONTAINER: Red<br />

SPECIAL HANDLING: Do NOT collect specimen in gel barrier tube<br />

SPECIMEN VOLUME: 3 mL<br />

MINIMUM VOLUME: 2 mL<br />

TEST AVAILABILITY: Daily<br />

TURNAR<strong>OU</strong>ND TIME: 1 month<br />

REFERENCE RANGE: Negative<br />

METHODOLOGY: Enzyme Linked Immuno-Sorbent Assay (ELISA)<br />

CPT: 83516<br />

[FHM] FAMILIAL HEMIPLEGIC MIGRAINE

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