Question 1

Purpose of the Procedure

Accepted Answer

Detecting rare genetic syndromes missed by traditional karyotyping. Diagnosing causes of structural anomalies found on ultrasound. Providing definitive genetic information for high-risk pregnancies.

Question 2

Who Should Get This Test?

Accepted Answer

Pregnant women with abnormal fetal ultrasound findings. Couples with a family history of chromosomal abnormalities. Cases with abnormal results from initial prenatal screening tests.

Question 3

Advantages of CMA Technology

Accepted Answer

100 times higher resolution than standard karyotyping. Detects submicroscopic deletions and duplications in DNA. Assists in specialized medical planning for birth and neonatal care.

Ensure Your Baby's Genetic Health - Fetal Chromosomal Microarray Analysis (CMA)