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Prenatal chromosome DEB assay test for Fanconi anemia risk during pregnancy

Prenatal Fanconi Anemia Chromosome Breakage Test

Chromosome Analysis, DEB Assay for Fanconi Anemia, Prenatal

  • Screen unborn baby for genetic risk
  • Detect inherited chromosome breakage patterns
  • Assess family history related risks
$4926
First results as soon as overnight*
Example results

All results normal? Get your money back. First-time customers only. File a support ticket titled “Money Back Guarantee” with your order number within 15 days of receiving your results. STD, Sickle Cell, and gift orders aren’t eligible. Full terms apply. guarantee
No questions asked refunds
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Prescription & all lab fees included

Go directly to the lab, no extra fees

Doctor's guidance included

Easy to understand results

Fast & convenient

Lab visit as quick as 10 mins in & out

Prescription & all lab fees included

Go directly to the lab, no extra fees

Doctor's guidance included

Easy to understand results

Fast & convenient

Lab visit as quick as 10 mins in & out

All results normal? Get your money back. First-time customers only. File a support ticket titled “Money Back Guarantee” with your order number within 15 days of receiving your results. STD, Sickle Cell, and gift orders aren’t eligible. Full terms apply. guarantee
No questions asked refunds
LegitScript certified

What's this test for?

This test is ideal if you're pregnant and have a family history of Fanconi anemia, or if you and your partner are known or suspected carriers of the condition. It helps identify whether the developing baby has inherited the genetic changes that cause Fanconi anemia, a rare blood disorder. This is often recommended when a previous child or close relative has been diagnosed with the condition.

What's included in this test?

This test uses a specialized technique called a DEB (diepoxybutane) assay to look at how a sample's chromosomes respond to a chemical stressor. Cells from people with Fanconi anemia show unusually high rates of chromosome breaks and rearrangements when exposed to DEB, which is why this method is considered a reliable way to detect the condition. This single assay is designed specifically to answer one question: does the baby show the chromosome fragility pattern associated with Fanconi anemia?

What happens after I get my results?

Your results will be available in your account, with an explanation of what the findings mean for your pregnancy. If the test shows signs of chromosome breakage consistent with Fanconi anemia, the report will outline next steps, which may include additional confirmatory testing or specialist follow-up. You can download a standard lab report directly from your account at any time. Because this is a one-time prenatal test, tracking over time typically isn't needed, but your account keeps a permanent record for your files.

Who should consider this test?
This test is best suited for pregnant individuals who already know that Fanconi anemia runs in their family, or whose partner is a known carrier. It's also appropriate if a genetic counselor or prior testing has flagged an increased risk based on family history. If there's no known family history or risk factor, this specialized test usually isn't necessary.
What symptoms indicate I may need this test?
Fanconi anemia doesn't cause symptoms in an unborn baby that you could notice yourself, so this test is driven by family history rather than symptoms you'd feel during pregnancy. Signs that prompt testing usually come from a family member's diagnosis, such as unexplained bone marrow failure, unusual bruising or bleeding in early childhood, or certain birth differences seen in relatives. If any blood relative has been diagnosed with Fanconi anemia, that history alone is a reason to consider this test, even without any symptoms of your own.
When will I get my results?
Results are typically ready within about 7 days after your sample is processed at the lab. Because this test involves growing and analyzing living cells, it takes a bit longer than routine blood work, so plan for about a week's turnaround. You'll be notified as soon as your results are posted to your account.
What is Fanconi anemia and why does it matter?
Fanconi anemia is a rare inherited condition that affects the body's ability to repair damaged DNA, which can lead to bone marrow failure, an increased risk of certain cancers, and physical differences present at birth. It matters during pregnancy because early knowledge allows families to plan for specialized newborn care and monitoring right from birth. Catching it prenatally means the right specialists and support can be lined up before delivery instead of after a diagnosis is made later.
What does a positive result mean?
A positive result means the baby's cells showed the chromosome breakage pattern typical of Fanconi anemia, suggesting the baby has inherited the condition. This doesn't predict exactly how severe symptoms will be, since Fanconi anemia can vary widely from person to person. It's a good idea to seek guidance promptly so a care plan can be in place for after the baby is born.
What causes Fanconi anemia to occur?
Fanconi anemia is caused by inherited mutations in one of several genes responsible for repairing broken DNA strands. A baby typically needs to inherit a mutated copy of the gene from both parents to develop the condition, which is why it often shows up when both parents happen to be carriers without knowing it. It's a genetic condition present from conception, not something caused by anything during pregnancy itself.
What should I do if my results are abnormal?
If your results show signs of Fanconi anemia, the report will explain the finding and suggest confirmatory follow-up steps. It's a good idea to connect with a genetic counseling resource to understand what the diagnosis means for your specific situation and to start planning for specialized newborn monitoring. Keep a copy of your downloadable report handy, as you'll likely want to share it when arranging follow-up care after delivery.
How’s this work?
Getting your blood test with us is easy, private & backed by the power of science.

Long story short:
  1. In the test options, use the filters or search box to narrow your choices and find the test you want.
  2. If you need a hand navigating through options, text our super friendly support team at 754-799-7833, and we'll provide tailored suggestions to help you find the ideal test.
  3. Once your order is placed, we’ll create your doctor’s lab order remotely, without any need for you to make a trip to a doctor in person or to talk to the doctor. Expect to receive your doctor’s lab order right in your inbox. It will also be in your patient portal if you need to find it later. We’ll also include instructions regarding fasting and other requirements for your test. Your patient portal will be auto-created hassle-free during checkout.
  4. If this is your first time ordering, you'll be prompted to create a password for instant login access to your patient portal. It's a quick way to conveniently access your orders and results whenever you want.
  5. When you’re ready, visit one of our 4,000 locations. Just bring your ID – no printing or faxing of your lab order is needed, as your order and details will already be in the lab system.
  6. Note that most lab locations don’t accept walk-ins, so it’s best to book an appointment in advance. Don’t worry – we’ll provide detailed instructions along the way.
  7. You’ll get your results via email & SMS and dive into understanding your body better. Yup, that easy!
  8. If you have any questions, please text us at 754-799-7833 or email [email protected] and we'll gladly help you.
How do I know which test to get?
In the test options, find the test you want. If you’re not sure which test to get, we can lend a hand in finding the right option.

Just text or call us at 754-799-7833, email us at [email protected], and we'll gladly help you. We've got your back and reply quickly.
Is it possible to make changes to my lab order if I made a mistake with the name, date of birth, or any other details?
Absolutely! We totally understand that errors can happen. No worries, we're here to help you.

Just reach out to us via text at 754-799-7833 or shoot us an email at [email protected]. Remember to include your order number and let us know the correct information you’d like to update. Our awesome team will jump right in and make sure everything is sorted out and accurate for you.

There are no changes necessary if your address is wrong on the requisition though. We don’t mail anything out.

Our lab requires an address to be listed to generate an order.
Do you accept health insurance?
Only HSA & FSA is accepted.

Our services are strictly self-pay and cannot be submitted to your health insurance provider except for Health Savings Accounts or Flexible Savings Accounts.

This policy applies to all insurance companies, including federal health insurance programs like Medicare.

If you have any questions, please text us at 754-799-7833 or email [email protected].
Can I cancel my order?
Yes.

We get it – sometimes your needs change.

As long as your samples haven’t been collected yet, we’re happy to help you cancel your order.

If you have any further questions, please text us at 754-799-7833 or email [email protected].

You can read more about our cancellation policy here.
How can I find a lab location near me?
During the ordering process, you’ll be able to select a specific lab near you, with no strings attached! You can switch it up later easily and visit any of our authorized locations as long as it’s the same lab company you selected your test for (Quest Diagnostics or Labcorp).

Before you proceed with your order, feel free to browse through all our lab locations here. This will give you the peace of mind of knowing that there's a lab nearby your home, office or your favorite gym.

If you have any questions, please text us at 754-799-7833 or email [email protected] and we'll gladly help you.

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Demo results
Chromosome Breakage (DEB Assay) Negative
Demo results
Negative (Normal) Positive (Breakage Detected)
Negative

What this means

A negative result means the baby's cells did not show the abnormal chromosome breakage pattern associated with Fanconi anemia. This suggests the baby is unlikely to have Fanconi anemia, though it does not test for every possible genetic condition. Your full report explains the finding in more detail.

* Regular blood test results (e.g., CBC) typically start arriving the next business day after sample collection. More advanced tests may take longer due to complexity.
Here’s how easy it is to get blood work done on your terms
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Prenatal Fanconi Anemia Chromosome Breakage Test

  • Screen unborn baby for genetic risk
  • Detect inherited chromosome breakage patterns
  • Assess family history related risks
$4926
Still got questions? Text our super-cool support team at 754-799-7833 to get help finding your ideal checkup.
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For informational purposes only. Not medical advice.