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Printable Test Catalog - OU Medicine

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METHODOLOGY: Enzyme-linked immunosorbent assay (ELISA)<br />

CLINICAL USE: Levels may be elevated in sepsis, autoimmune<br />

diseases, various infectious diseases and<br />

transplant rejection<br />

CPT: 83520<br />

[TWIST] CRANIOSYN/SAETHRE-CHOTZEN(TWIS<br />

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

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

SPECIMEN VOLUME: 2 tubes of 3-5 mL (children & adults)<br />

MINIMUM VOLUME: 1-2 mL (newborn)<br />

TEST AVAILABILITY: Daily<br />

TURNAR<strong>OU</strong>ND TIME: 15-20 days<br />

METHODOLOGY: PCR amplification and DNA sequencing<br />

CLINICAL USE: Confirm the nature of the dwarfism in affected<br />

individual; Determine whether Saethre-Chotzen<br />

syndrome is responsible for abnormalities in skull<br />

eyes, or limbs; Discriminate between syndromes<br />

with different but overlapping clinical symptoms<br />

in affected individual; To establish whether<br />

symptoms are spontaneous or inherited within a<br />

family; Evaluate risk of having a child with<br />

Saethre-Chotzen Syndrome<br />

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

[TXUA] UA FOR TRANSFUSION REACTION<br />

[TYPHUS] TYPHUS FEVER GR<strong>OU</strong>P-RICKETTSIA<br />

SPECIMEN REQUIRED: Refrigerated serum<br />

TUBE OR CONTAINER: Red or Gold<br />

SPECIMEN VOLUME: 2 mL<br />

MINIMUM VOLUME: 1 mL<br />

TEST INCLUDES: IgG and IgM<br />

TEST AVAILABILITY: Daily<br />

METHODOLOGY: Immunofluorescence (IF)<br />

CPT: 86757 x 2<br />

[TYROS] Tyrosine Level<br />

SPECIMEN REQUIRED: Frozen plasma<br />

TUBE OR CONTAINER: Green (heparin)<br />

SPECIMEN VOLUME: 4 mL<br />

MINIMUM VOLUME: 0.5 mL<br />

TEST AVAILABILITY: Daily<br />

TURNAR<strong>OU</strong>ND TIME: 7-9 days<br />

REFERENCE RANGE: Neonate: < 1 month: 3.9-12.9 umol/dL<br />

1 month - 16 years: 3.3-11.9 umol/dL<br />

Adult: > 16 years: 3.2-12.2 umol/dL<br />

METHODOLOGY: High-Pressure Liquid Chromatography (HPLC)<br />

CLINICAL USE: Detection of a specific amino acid deficiency<br />

CPT: 82131

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