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 Chromosomal Microarray Analysis (CMA) is an advanced prenatal diagnostic tool that detects microdeletions, duplications, aneuploidy, and submicroscopic abnormalities. With higher resolution than karyotyping, CMA offers superior diagnostic capability. It is recommended for POC testing, aneuploidy screening, and detecting ASD and MCA. Samples include amniotic fluid, EDTA blood, or POC with a 15-day turnaround time. CMA enables informed decision-making for expectant parents.