Purpose of the Procedure
- Detecting rare genetic syndromes missed by traditional karyotyping.
- Diagnosing causes of structural anomalies found on ultrasound.
- Providing definitive genetic information for high-risk pregnancies.
Book Fetal Chromosomal Microarray (CMA) | Lahalak Medical Platform
A sophisticated, high-resolution genetic test providing peace of mind by detecting microscopic chromosomal abnormalities in the fetus, ensuring early detection of genetic disorders that standard testing might miss for a healthy pregnancy.
Scientific name: Fetal Chromosomal Microarray Analysis (CMA)
A high-resolution genetic test using microarray technology to detect submicroscopic chromosomal gains or losses (CNVs) via amniocentesis, providing a comprehensive evaluation of fetal genetic health and developmental risks.
Service type
Advanced Genetic Testing
Duration
20-30 minutes
Fasting
Fasting is not required
Included Services
- Ultrasound-guided amniocentesis
- Microarray analysis
- Comprehensive genetic report
Medical Service Information
Who Should Get This Test?
- Pregnant women with abnormal fetal ultrasound findings.
- Couples with a family history of chromosomal abnormalities.
- Cases with abnormal results from initial prenatal screening tests.
Advantages of CMA Technology
- 100 times higher resolution than standard karyotyping.
- Detects submicroscopic deletions and duplications in DNA.
- Assists in specialized medical planning for birth and neonatal care.
Conditions & Notices
- Requires prior medical consent from a fetal specialist
- Typically performed between weeks 15 and 20 of pregnancy
Medical services you might also like
