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BAYLOR GENETICS 2450 HOLCOMBE BLVD. GRAND BLVD. RECEIVING DOCK HOUSTON, TX 770212024PHONE 1.800.411.4363 FAX 1.800.434.9850CONNECTPRENATAL CHROMOSOMAL MICROARRAY ANALYSIS (CMA) & CYTOGENETICS REQUISITION
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How to fill out prenatal chromosomal microarray analysis

01
Collect the necessary information and medical history from the patient.
02
Obtain a sample of fetal cells for analysis, typically through chorionic villus sampling (CVS) or amniocentesis.
03
Extract the DNA from the fetal cells using appropriate laboratory techniques.
04
Prepare the DNA sample for microarray analysis by labeling it with fluorescent markers.
05
Apply the labeled DNA sample to a microarray chip containing thousands of specific DNA probes.
06
Allow the DNA to hybridize with the probes on the chip and wash away any unbound DNA.
07
Use a scanning device to detect the fluorescent signals emitted by the labeled DNA on the chip.
08
Analyze the detected signals to determine the presence or absence of chromosomal abnormalities.
09
Interpret the results and provide a detailed report to the healthcare provider.

Who needs prenatal chromosomal microarray analysis?

01
Prenatal chromosomal microarray analysis is recommended for pregnant individuals who:
02
- Have advanced maternal age (35 years or older)
03
- Have had a previous pregnancy with chromosomal abnormalities
04
- Have a family history of genetic disorders or chromosomal abnormalities
05
- Have abnormal ultrasound findings suggestive of a chromosomal abnormality
06
- Have a positive screening test result for chromosomal abnormalities
07
- Elect to undergo further genetic testing for their own peace of mind
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Prenatal chromosomal microarray analysis is a genetic test that detects extra or missing chromosomal segments in a developing fetus.
Prenatal chromosomal microarray analysis may be recommended for pregnant women with certain risk factors or abnormal ultrasound findings.
Prenatal chromosomal microarray analysis is typically performed by a healthcare provider using a blood sample from the pregnant woman or amniotic fluid.
The purpose of prenatal chromosomal microarray analysis is to detect genetic abnormalities in the fetus that may impact its development or health.
Prenatal chromosomal microarray analysis reports typically include details on chromosomal abnormalities detected, as well as recommendations for further testing or management.
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