Description
Chromosomal Microarray Analysis (CMA) is a sophisticated genetic test that examines the entire genome for small chromosomal deletions, duplications, and rearrangements. It offers higher resolution than traditional karyotyping, allowing for the detection of submicroscopic chromosomal abnormalities. CMA is particularly useful in diagnosing genetic causes of developmental delays, intellectual disabilities, autism spectrum disorders, and multiple congenital anomalies. The test can identify both known genetic syndromes and novel genomic imbalances. Results from CMA can provide crucial information for genetic counseling, prognosis, and tailored medical management.
Reviews
There are no reviews yet.