Get the free Prenatal Trio Whole Exome Sequencing Requisition Prenatal Trio Whole Exome Sequencin...

BAYLOR MARACA GENETICS LABORATORIES SHIP TO: Baylor Maraca Genetics Laboratories 2450 Holcombe, Grand Blvd. Receiving Dock Houston, TX 770212024 Phone: 7137986555 PHONE: 800411GENE FAX: 7137982787

How to fill out prenatal trio whole exome

How to fill out prenatal trio whole exome:

1. Obtain the necessary forms: Contact the laboratory or healthcare provider who will be conducting the prenatal trio whole exome sequencing to obtain the relevant forms. These forms typically include patient information, consent forms, and any additional instructions.
2. Complete the patient information: Provide accurate and detailed information about the pregnant individual, the biological father, and the fetus. This may include personal details such as name, date of birth, and contact information.
3. Consent and authorization: Read and sign the necessary consent forms, which outline the purpose and potential risks of the prenatal trio whole exome sequencing. Ensure that both parents or legal guardians consent to the procedure if applicable.
4. Provide medical history: Fill out any sections of the form requesting medical history information, including any relevant medical conditions, previous pregnancies, or family history of genetic disorders. This information can help guide the analysis and interpretation of the sequencing results.
5. Gestational age and sample collection: Indicate the gestational age of the fetus at the time of sample collection. Follow the specific instructions provided by the laboratory or healthcare provider to collect the required samples, which usually involve a blood sample from the pregnant individual, a saliva or blood sample from the biological father, and a fetal sample which can be obtained through amniocentesis or chorionic villus sampling.
6. Shipping and logistics: Coordinate with the laboratory or healthcare provider regarding the proper packaging, handling, and shipping of the samples. Follow any specific instructions provided to ensure the samples remain viable during transit.
7. Payment and insurance: Determine the cost of the prenatal trio whole exome sequencing and explore any possible insurance coverage. Complete the necessary sections regarding payment and insurance information, providing accurate details to avoid any delays or complications.

Who needs prenatal trio whole exome:

1. Parents with a family history of genetic disorders: Individuals with a family history of certain genetic disorders may opt for prenatal trio whole exome sequencing to assess the risk of the disorder in their unborn child. This can help them make informed decisions about their pregnancy and potential treatment options.
2. Couples with recurrent pregnancy loss: Couples who have experienced repeated miscarriages or pregnancy loss may choose prenatal trio whole exome sequencing to investigate potential genetic causes. Identifying any underlying genetic abnormalities can aid in understanding the reasons behind the pregnancy loss and guide future reproductive decisions.
3. Individuals with abnormal prenatal screening results: If routine prenatal screening tests, such as ultrasound or blood tests, indicate a potential genetic abnormality or increased risk, prenatal trio whole exome sequencing may be recommended. The analysis of the exome can provide a more comprehensive understanding of any genetic variations or abnormalities present in the fetus.
4. Those seeking reassurance and peace of mind: Some parents may choose prenatal trio whole exome sequencing simply as a proactive measure to ensure the health and well-being of their unborn child. The comprehensive nature of the test allows for a thorough evaluation of the fetus's genetic makeup, providing reassurance and peace of mind during the pregnancy journey.

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