Chromosome Analysis (Karyotyping)
- Also Known As:
- Karyotype
- Cytogenetics
- Cytogenetic Analysis
- Chromosome Studies
- Chromosome Karyotype

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At a Glance
Why Get Tested?
To detect chromosome abnormalities, thus to help diagnose genetic diseases, some birth defects, and certain disorders of the blood and lymphatic system
When To Get Tested?
When pregnancy screening tests are abnormal; whenever signs of a chromosomal abnormality-associated disorder are present; as indicated to detect chromosomal abnormalities in a person and/or detect a specific abnormality in family members; sometimes when a person has leukemia, lymphoma, myeloma, myelodysplasia or another cancer and an acquired chromosome abnormality is suspected
Sample Required?
A blood sample drawn from a vein in your arm; a sample of amniotic fluid or chorionic villus from a pregnant woman; a bone marrow or tissue sample
Test Preparation Needed?
None
What is being tested?
Chromosome analysis or karyotyping is a test that evaluates the number and structure of a person’s chromosomes in order to detect abnormalities. Chromosomes are thread-like structures within each cell nucleus and contain the body’s genetic blueprint. Each chromosome contains thousands of genes in specific locations. These genes are responsible for a person’s inherited physical characteristics and they have a profound impact on growth, development, and function.
Humans have 46 chromosomes, present as 23 pairs. Twenty-two pairs are found in both sexes (autosomes) and one pair (sex chromosomes) is present as either XY (in males) or XX (in females). Normally, all cells in the body that have a nucleus will contain a complete set of the same 46 chromosomes, except for the reproductive cells (eggs and sperm), which contain a half set of 23. This half set is the genetic contribution that will be passed on to a child. At conception, half sets from each parent combine to form a new set of 46 chromosomes in the developing fetus.
Chromosomal abnormalities include both numerical and structural changes. For numerical changes, anything other than a complete set of 46 chromosomes represents a change in the amount of genetic material present and can cause health and development problems. For structural changes, the significance of the problems and their severity depends upon the chromosome that is altered. The type and degree of the problem may vary from person to person, even when the same chromosome abnormality is present.
A chromosomal karyotyping examines a person’s chromosomes to determine if the right number is present and to determine if each chromosome appears normal. It requires experience and expertise to perform properly and to interpret the results. While theoretically almost any cells could be used to perform testing, in practice it is usually performed on amniotic fluid to evaluate a fetus and on lymphocytes (a white blood cell) from a blood sample to test all other ages. Alternately, white blood cells may be obtained from bone marrow aspirations to look for changes in individuals suspected of having hematologic or lymphoid diseases (e.g., leukemia, lymphoma, myeloma, refractory anemia).
The test is performed by:
- Taking a sample of a person’s cells, culturing them in nutrient-enriched media to promote cell division in vitro. This is done in order to select a specific time during the cells’ growth phase when the chromosomes are easiest to distinguish.
- Isolating the chromosomes from the nucleus of the cells, placing them on a slide, and treating them with a special stain.
- Taking microphotographs of the chromosomes.
- In jigsaw puzzle fashion, rearranging the pictures of the chromosomes to match up pairs and arrange them by size, from largest to smallest, numbers 1 to 22, followed by the sex chromosomes as the 23rd pair.
- The pictures also allow the chromosomes to be vertically oriented. Each chromosome looks like a striped straw. It has two arms that differ in length (a short arm (p) and a long arm (q)), a pinched-in area between the arms called a centromere, and a series of light and dark horizontal bands. The length of the arms and the location of the bands help determine top from bottom.
- Once the chromosome photo arrangement is completed, a laboratory specialist evaluates the chromosome pairs and identifies any abnormalities that may be present.
Some chromosomal disorders that may be detected include:
- Down syndrome (Trisomy 21), caused by an extra chromosome 21; this may occur in all or most cells of the body.
- Edwards syndrome (Trisomy 18), a condition associated with severe mental retardation; caused by an extra chromosome 18.
- Patau syndrome (Trisomy 13), caused by an extra chromosome 13.
- Klinefelter syndrome, the most common sex chromosome abnormality in males; caused by an extra X chromosome.
- Turner syndrome, caused by missing one X chromosome in females.
- Chronic myelogenous leukemia, a classic 9;22 translocation that is diagnostic of the disease.
How is the sample collected for testing?
- A blood sample is obtained by inserting a needle into a vein in the arm.
- Amniotic fluid and chorionic villi are collected from a pregnant woman by a healthcare practitioner using amniocentesis or chorionic villus sampling procedures.
- Bone marrow or tissue sample collections require a biopsy procedure to be performed.
Common Questions
View Sources
Sources Used in Current Review
Tietz Textbook of Clinical Chemistry and Molecular Diagnostics. Burtis CA, Ashwood ER, Bruns DE, eds. 4th edition, St. Louis: Elsevier Saunders; 2006, Pp 1466-1474.
(April 24, 2014) Petrozza J. Recurrent Early Pregnancy Loss. Medscape Reference. Available online at http://emedicine.medscape.com/article/260495-overview. Accessed April 2016.
Henry’s Clinical Diagnosis and Management by Laboratory Methods. 22nd ed. McPherson R, Pincus M, eds. Philadelphia, PA: Saunders Elsevier: 2011, Pp 1293-1312.
(©2016) Mayo Clinic. Chromosome Analysis, Congenital Disorders, Blood. Available online at http://www.mayomedicallaboratories.com/test-catalog/Clinical+and+Interpretive/35248. Accessed April 2016.
(©2016) Mayo Clinic. Chromosome Analysis, Hematologic Disorders, Blood. Available online at http://www.mayomedicallaboratories.com/test-catalog/Overview/35308. Accessed April 2016.
Sources Used in Previous Reviews
Haldeman-Englert, C. (Updated 2010 December 1). Karyotyping. MedlinePlus Medical Encyclopedia [On-line information]. Available online at http://www.nlm.nih.gov/medlineplus/ency/article/003935.htm. Accessed October 2011.
(© 1996-2011). Introduction to Chromosomes. Chromosome Disorder Outreach. [On-line information]. Available online at http://www.chromodisorder.org/CDO/General/IntroToChromosomes.aspx. Accessed October 2011.
(2011 October 4). Handbook, Help me Understand Genetics. Genetics Home Reference, [On-line information]. Available online at http://ghr.nlm.nih.gov/handbook. Accessed October 2011.
Manning, M. and Hudgins, L. (2010 November). Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities. ACMG Practice Guidelines Genetics In Medicine v 12 (11) [On-line information]. PDF available for download at http://www.acmg.net/StaticContent/PPG/Array_based_technology_and_recommendations_for.13.pdf. Accessed October 2011.
(© 1995–2011). Unit Code 8696: Chromosome Analysis, for Congenital Disorders, Blood. Mayo Clinic Mayo Medical Laboratories [On-line information]. Available online at http://www.mayomedicallaboratories.com/test-catalog/Overview/8696. Accessed October 2011.
Liptak, G. (Revised 2009 January). Overview of Chromosomal Anomalies. Merck Manual for Healthcare Professionals [On-line information]. Available online through http://www.merckmanuals.com. Accessed October 2011.
(2009 December). Chromosomal abnormalities. March of Dimes [On-line information]. Available online at http://www.marchofdimes.com/baby/birthdefects_chromosomal.html. Accessed October 2011.
(© 2011). Using Karyotypes to Predict Genetic Disorders. Learn. Genetics Genetic Science Learning Center, University of Utah [On-line information]. Available online at http://learn.genetics.utah.edu/content/begin/traits/predictdisorder/. Accessed October 2011.
Pagana, K. D. & Pagana, T. J. (© 2011). Mosby’s Diagnostic and Laboratory Test Reference 10th Edition: Mosby, Inc., Saint Louis, MO. Pp 268-269.
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