What is the Chromosome Blood Routine Test?
The Chromosome Blood Routine test, also known as a karyotype test, analyzes the structure and number of chromosomes in your blood cells. It may help identify genetic disorders by detecting abnormalities in the chromosomes.
Why is the Chromosome Blood Routine Test Important?
This test is crucial in both medicine and functional medicine. In medicine, it may aid in diagnosing genetic conditions such as Down syndrome, Klinefelter syndrome, and other chromosomal abnormalities. In functional medicine, it may provide insights into genetic factors affecting your overall health and well-being. Talk to your primary healthcare physician about these genetic conditions.
Why Should You Consider Ordering this Test?
Ordering this test may provide valuable information about your genetic makeup. It may help you understand the risk of inherited conditions, plan for family health, and make informed decisions about your medical care. Early detection of chromosomal abnormalities can lead to timely interventions and better health outcomes.
Labs Included in Your Order
| Test Name | Reference Range | Low and High Levels of Chromosome |
|---|---|---|
| Chromosome Analysis, Whole Blood |
|
High: High levels of chromosomal abnormalities may indicate genetic disorders like Down syndrome or Klinefelter syndrome.
Low: Low levels are not typically applicable for chromosome count but deviations in structure or number can indicate genetic issues. |
Chromosome, Blood Routine FAQs
What is the Chromosome Blood Routine Test for?
This test is used to analyze the structure and number of chromosomes in your blood cells. It may help detect genetic abnormalities that may cause various genetic disorders and health issues.
What do low and high levels mean?
High Levels: High levels of chromosomal abnormalities may indicate genetic disorders such as Down syndrome, Klinefelter syndrome, or Turner syndrome.
Low Levels: Low levels typically refer to deviations in chromosome structure or number, which can also signify genetic problems but are not applicable in the same way as chemical biomarkers.
We recommend reaching out to your primary healthcare provider when your results show either high or low levels.
What are the signs and symptoms of the issues the test is testing for?
Signs and symptoms may vary based on the specific genetic disorder. Common indicators may include developmental delays, intellectual disabilities, physical malformations, infertility, and other health issues related to genetic abnormalities. Reach out to your primary healthcare provider if these symptoms are present.
How often should I retest?
Retesting is usually not required unless advised by your healthcare provider. It may be necessary if there are changes in health conditions or if a more detailed analysis is needed.
How accurate is the test?
This test is highly accurate for detecting chromosomal abnormalities. However, false positives or negatives may occur due to genetic variants or other factors like recent blood transfusions.
Are test results private and confidential?
Receive test results securely on TrueHealthLabs.com under ‘My Account.’ It’s critical that you share them with your physician. Results may be disclosed to health authorities only if legally mandated, e.g., for STDs or COVID-19. Review our privacy policy for more details.
To learn more, see our comprehensive guide to the Chromosome Blood Routine Test.
Medical Review Board
Reviewed by our medical review board consisting of Jeff Donohue M.D. from Body Logic and Brady Hurst DC, CCCN. Written by True Health Labs team of editorial health contributors.
Disclaimer: This information is for educational purposes only and not intended as medical advice. Consult your healthcare provider for personalized guidance.
