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Chromosome Analysis, Chorionic Villus Sample
Test Code14592
CPT Codes
88235, 88267, 88280
Physician Attestation of Informed Consent
This germline genetic test requires physician attestation that patient consent has been received if ordering medical facility is located in AK, DE, FL, GA, IA, MA, MN, NV, NJ, NY, OR, SD or VT or test is performed in MA.
Preferred Specimen
40 mg chorionic villi in Hanks', Ringer's solution or culture medium with antibiotics
Minimum Volume
20 mg
Instructions
Ship in sterile container in Hanks', Ringer's solution or culture medium with antibiotics. CVS media available upon request. Ship at room temperature.
Please contact the laboratory Genetic Counselor at 1-866-GENEINFO (1-866-436-3463) with any questions.
Specimen viability decreases during transit. Send specimen to testing lab for viability determination. Do not freeze. Do not reject.
Please contact the laboratory Genetic Counselor at 1-866-GENEINFO (1-866-436-3463) with any questions.
Specimen viability decreases during transit. Send specimen to testing lab for viability determination. Do not freeze. Do not reject.
Transport Temperature
Room temperature
Specimen Stability
Room temperature: Preferred
Refrigerated: Acceptable
Frozen: Unacceptable
Refrigerated: Acceptable
Frozen: Unacceptable
Methodology
Culture • Microscopy • Karyotype
Setup Schedule
Set up: Mon-Sat; Report available: 8 days
Limitations
Chromosome aberrations observed in the CVS specimen but not in the fetus (confined placental mosaicism) occurs in approximately 1% of cases.
Reference Range
Interpretive report
Clinical Significance
This test will detect chromosome abnormalities of the fetus including numerical, structural, and mosaic abnormalities. Chromosome analysis will also reveal fetal gender and sex chromosome abnormalities. Indications for prenatal chromosome analysis may include advanced maternal age, abnormal fetal ultrasound, abnormal maternal serum screen, abnormal cell-free DNA results, history of a previous child with a chromosome abnormality, or a parent who carries a balanced chromosomal rearrangement or has another chromosome abnormality.