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Tag: genetic testing

  • The Quad Screen Test: What You Should Know

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    Read more The Quad Screen test is a blood test that provides insights into the health of your developing baby by measuring four key substances in your blood. It helps assess the likelihood of certain genetic conditions and can be a valuable part of your prenatal care. When is the Quad Screen Test Done? Typically,…

  • What is Chorionic Villus Sampling (CVS)?

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    Read more If you’re at an increased risk of having a baby with chromosomal disorders or other birth defects, your healthcare provider might suggest a genetic test known as chorionic villus sampling, or CVS. This test is performed in the first trimester and involves collecting a small tissue sample from the chorionic villi, which are…

  • Preimplantation Genetic Diagnosis: Understanding the Process and Its Implications

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    Read more Preimplantation Genetic Diagnosis (PGD) is a medical procedure designed to identify genetic defects in embryos created through in vitro fertilization (IVF). This screening helps prevent certain genetic conditions from being passed on to a child. How Does PGD Work? The process of PGD begins with the standard IVF procedure, which involves retrieving eggs…

  • Prenatal Testing: What You Need to Know

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    Read more Prenatal testing is crucial for understanding your health and identifying potential issues during pregnancy. These tests provide valuable insights into the likelihood of birth defects or genetic diseases, enabling you to make informed healthcare choices for you and your baby. While some tests are recommended for all expectant mothers, others may be necessary…

  • Cystic Fibrosis (CF) and Pregnancy: What You Need to Know

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    Read more If you’ve been managing cystic fibrosis (CF) for a while, you’re likely familiar with the unique challenges that come with it. But when it comes to pregnancy, there’s no need to feel overwhelmed. With the right support and care, you can navigate this journey successfully, ensuring the well-being of both you and your…

  • Chorionic Villus Sampling (CVS) Explained

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    Read more Chorionic Villus Sampling, commonly referred to as CVS, is a diagnostic procedure utilized to detect chromosomal abnormalities and genetic disorders in a developing fetus. If there’s a history of genetic issues in your family, your healthcare provider might recommend this test. How is CVS Performed? CVS is a minimally invasive procedure where a…

  • First Trimester Screening

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    Read more The First Trimester Screening is an optional, non-invasive evaluation that combines a maternal blood test with an ultrasound to assess the risk of certain chromosomal abnormalities, such as Down Syndrome (Trisomy 21) and Trisomy 18. This screening also includes an assessment of nuchal translucency, which can help detect other significant fetal issues, including…