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Sagot :
Answer:Karyotyping is a laboratory procedure that allows your doctor to examine your set of chromosomes. “Karyotype” also refers to the actual collection of chromosomes being examined. Examining chromosomes through karyotyping allows your doctor to determine whether there are any abnormalities or structural problems within the chromosomes.
Explanation:
An unusual number of chromosomes, incorrectly arranged chromosomes, or malformed chromosomes can all be signs of a genetic condition. Genetic conditions vary greatly, but two examples are Down syndrome and Turner syndrome. Karyotyping can be used to detect a variety of genetic disorders.
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