Biomarkers · Chemical
CAH (21-Hydroxylase Deficiency) Common Mutations, Fetal Cells
- LOINC codes
- 48781-9
- Tests that measure CAH (21-Hydroxylase Deficiency) Common Mutations, Fetal Cells
- Quest Diagnostics 1
Tests
Check the catalog code, specimen, method and preparation for every test that measures CAH (21-Hydroxylase Deficiency) Common Mutations, Fetal Cells. Select up to five tests to compare them side by side.
Quest Diagnostics 1 test
Single-analyte tests
CAH (21-Hydroxylase Deficiency) Common Mutations, Fetal Cells 91680
10 mL amniotic fluid collected in a sterile plastic leak-proof container · Fasting not stated · Turnaround Set up: Tues
Quest Diagnostics catalog pageMethod and collection
- Method
- Electrophoresis • Minisequencing • Polymerase Chain Reaction (PCR)
- Collection
- Do not hold specimen; Forward to laboratory when specimen arrives. Amniotic fluid: Normal collection procedure. Specimen stability is crucial. Store and ship at room temperature immediately. Do not refrigerate or freeze; Forward to laboratory when sample arrives. 1. Please call 1-866-GENE-INFO (1-866-436-3463) prior to submission. 2. Documentation of parental carrier status must be provided. 3. It is required that maternal cell contamination study, str analysis be ordered in conjunction with fetal testing. A separate tube of maternal blood (EDTA) is required for this test. Amniocyte or chorionic villus (CVS) culture: Two sterile T-25 flasks, 75% confluent, filled with culture medium. Specimen stability is crucial. Store and ship at room temperature immediately. Do not refrigerate or freeze; Forward to laboratory when cells arrive. Dissected chorionic villus (CVS) biopsy: 10-20 mg dissected chorionic villi collected in sterile tube, filled with sterile culture medium. Specimen stability is crucial. Store and ship at room temperature immediately. Do not refrigerate or freeze; Forward to laboratory when sample arrives.
- Reference notes
- See Laboratory Report
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Quest Diagnostics test catalog
1 test: codes, specimens, methods, preparation and reference intervals.
LOINC 48781-9
Regenstrief Institute codes that identify the same result across labs.
Search ClinicalTrials.gov for CAH (21-Hydroxylase Deficiency) Common Mutations, Fetal Cells
Registered studies that measure CAH (21-Hydroxylase Deficiency) Common Mutations, Fetal Cells, on the U.S. National Library of Medicine registry.
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We compile this page from named laboratory catalogs, guidelines and studies. Labs calculate reference intervals from the people they test, for one assay method and one population group, so an interval describes that population rather than an optimal target.
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