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Fanconi anemia group C occurs at an increased frequency in individuals of Ashkenazi Jewish descent, with a carrier frequency of 1 in 89. It is an inherited anemia that sometimes results in short stature, radial ray defects, cardiac and urogenital abnormalities and learning disabilities or mental retardation.

Couples who are planning a pregnancy or who are already pregnant may decide to have testing to find out if they are carriers and at risk of having a baby with Fanconi anemia group C. It is standard of care to offer carrier screening to individuals of Ashkenazi Jewish descent for Bloom syndrome, Canavan disease, cystic fibrosis, familial dysautonomia, Fanconi anemia group C, Gaucher disease, mucolipidosis type IV, Niemann-Pick disease type A and Tay-Sachs disease. If both parents are found to be carriers, prenatal diagnosis by CVS or amniocentesis is available. Our Fanconi anemia group C mutation analysis tests for 1 mutation for a 99% carrier detection rate in the Ashkenazi Jewish population.

Please Note: For an individual suspected of having Fanconi Anemia, chromosome breakage analysis should be considered in the diagnostic evaluation of the patient. Please refer to the Cytogenetics – Chromosome Breakage Analysis test page for additional information on specimen requirements.

CPT Codes:

83893(1), 83894(1), 83896(2), 83898(1)

1. Blood:
   • ACD-A (yellow-top) or EDTA (lavender-top) tube.
   • Adult: 10 ml whole blood; 30 ml whole blood if ordering multiple tests.
   • Turnaround Time:
     10-14 days
2. Mouthwash:
   • Please Note: Patient should not eat, drink, smoke or chew gum for at least one hour prior to collection. (See specimen kit for detailed instructions). Mouthwash samples can be sent when ordering up to two tests. When ordering more than two tests, blood samples are required.
   • 10 ml of Scope® mouthwash that has been swished vigorously for at least 1 minute.
   • Collect in orange-top 50 ml polypropylene tube.
   • Turnaround Time:
     10-14 days
3. Prenatal:
   • Please Note: Call a laboratory genetic coordinator prior to obtaining any prenatal specimens. Prenatal testing is recommended only for carrier couples with identified mutations. In some circumstances, specimens from other family members may be required.
     All prenatal specimens (including cord blood) must be accompanied by a maternal blood or mouthwash specimen for analysis of possible maternal cell contamination.
   • Discard first 2 ml; then 10 ml amniotic fluid in 15 ml orange-top polypropylene tube, 10-15 mg chorionic villi in laboratory-provided screw-top tubes with sterile transport medium or 1 T-25 flask of confluent cells.
   • Additional sample must be obtained for back-up culture at one of our cytogenetics laboratories or another facility.
   • If additional testing is desired, more amniotic fluid is needed. For example, chromosome analysis requires an additional 15-25 ml (see Cytogenetics – Amniotic Fluid Chromosome Analysis test page) and AFAFP requires an additional 2 ml (see Amniotic Fluid Alpha-Fetoprotein - AFAFP test page).
   • Turnaround Time:
     10-14 days (when cell culture required, add ~2 weeks)

Client Services: Reproductive/Genetics   800-848-4436

Specimen Services/Pickup:  877-246-1226