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BAYLOR GENETICS
2450 HOLCOMBE BLVD.
GRAND BLVD. RECEIVING DOCK
HOUSTON, TX 770212024PHONE
1.800.411.4363
FAX
1.800.434.9850CONNECTGENOME REANALYSIS REQUISITION
PATIENT INFORMATION (COMPLETE ONE FORM
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How to fill out prenatal chromosomal microarray analysis
How to fill out prenatal chromosomal microarray analysis
01
Collect a sample of the patient's blood or amniotic fluid.
02
Send the sample to a laboratory that specializes in genetic testing.
03
Fill out any necessary paperwork and provide relevant medical history.
04
Wait for the results to be processed and analyzed by a genetic counselor or healthcare provider.
05
Discuss the findings with the patient and provide guidance on next steps.
Who needs prenatal chromosomal microarray analysis?
01
Prenatal chromosomal microarray analysis is typically recommended for pregnant women who have had abnormal ultrasound findings, a previous child with a chromosomal abnormality, a family history of genetic disorders, or advanced maternal age.
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What is prenatal chromosomal microarray analysis?
Prenatal chromosomal microarray analysis is a test that can detect chromosomal abnormalities in a fetus before birth.
Who is required to file prenatal chromosomal microarray analysis?
Prenatal chromosomal microarray analysis is typically recommended for pregnant individuals who are at increased risk of having a child with a chromosomal abnormality.
How to fill out prenatal chromosomal microarray analysis?
Prenatal chromosomal microarray analysis is usually performed by a healthcare provider using a blood sample from the pregnant individual.
What is the purpose of prenatal chromosomal microarray analysis?
The purpose of prenatal chromosomal microarray analysis is to identify any chromosomal abnormalities in the fetus that may impact the baby's health or development.
What information must be reported on prenatal chromosomal microarray analysis?
The results of the prenatal chromosomal microarray analysis will report any chromosomal abnormalities found in the fetus.
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