Description
Chromosomal Microarray Analysis (CMA) is a sophisticated genetic test that examines the entire genome for small chromosomal deletions or duplications, known as copy number variations (CNVs). This high-resolution technique can detect genetic changes that are too small to be seen with traditional karyotyping. CMA is particularly useful in diagnosing developmental delays, autism spectrum disorders, and multiple congenital anomalies. It can also provide valuable information about the prognosis and potential health risks associated with specific genetic variations. The test results often require interpretation by a genetic counselor or specialist to fully understand their implications.
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