Comprehensively evaluate your chromosomes for potential abnormalities.
- 15 min15 minutes
- 550 British pounds£550
- 305 Neasden Lane, London NW10 1QR, UK
Molecular karyotype test, also known as chromosomal microarray analysis (CMA), detect small changes in a person's DNA that may be responsible for a variety of genetic disorders. The test involves analysing a person's DNA for the presence of microdeletions, microduplications, or other changes in the number or structure of chromosomes that may be too small to be detected by conventional karyotyping. Molecular karyotyping can be used to diagnose a wide range of genetic disorders, including developmental delays, intellectual disability, birth defects, and certain types of cancer. It can also be used to identify genetic causes of infertility, recurrent pregnancy loss, and other reproductive problems. Molecular karyotyping is a powerful tool for diagnosing genetic disorders, but it is important to note that not all genetic changes detected by the test will necessarily cause disease. Some genetic changes may be benign or of uncertain significance. Sample: BLOOD Results: 5 WEEKS Phlebotomy fee: Included in price Code: E-G25-5WKS
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305 Neasden Lane, London NW10 1QR, UK