Chromosome Analysis, 15-20 Cells, 2 Karyotypes Priced at $1,240 at Aurora Burlington
Aurora Medical Center Burlington offers a specialized medical service known as Chromosome Analysis, which involves examining 15-20 cells and producing two karyotypes to detect genetic abnormalities. This diagnostic procedure is crucial for identifying chromosomal disorders, which can aid in the diagnosis and management of various genetic conditions. The service is priced at $1,240, reflecting the complexity and precision required for such genetic testing. This analysis is particularly valuable for patients with unexplained developmental delays, congenital anomalies, or a family history of genetic disorders.
What is Chromosome Analysis? – Chromosome Analysis is a laboratory test that examines the chromosomes in a sample of cells to identify genetic abnormalities that may cause disease or developmental issues.
Why are 15-20 cells analyzed in this test? – Analyzing 15-20 cells ensures a comprehensive examination of the chromosomes, increasing the accuracy and reliability of the test results.
What is a karyotype? – A karyotype is a visual representation of an individual’s chromosomes, arranged and numbered by size, which helps in identifying any structural or numerical chromosomal abnormalities.
Who should consider getting this test? – Individuals with unexplained developmental delays, congenital anomalies, or a family history of genetic disorders may benefit from this test to identify potential genetic causes.
How is the test performed? – The test is performed by collecting a sample of cells, usually from blood, bone marrow, or amniotic fluid, which are then cultured and analyzed under a microscope to produce a karyotype.
What does the cost of $1,240 cover? – The cost of $1,240 covers the entire process of chromosome analysis, including cell culture, karyotyping, and interpretation of results by a genetic specialist.
How long does it take to get results? – Results from chromosome analysis typically take several days to a few weeks, depending on the complexity of the case and the laboratory’s workload.
Are there any risks associated with the test? – The risks are minimal, primarily related to the method of sample collection, such as slight discomfort or bruising from a blood draw.
Can this test detect all genetic disorders? – While chromosome analysis can identify many chromosomal abnormalities, it may not detect all genetic disorders, particularly those caused by small mutations or single-gene defects.
