Down syndrome is one of the most well-known genetic abnormalities, it’s crucial to remember that numerous other genetic conditions could impact pregnancies. Advancements in medical technology, such as prenatal genetic testing, provide valuable insights into potential genetic anomalies. This allows parents to make informed decisions about their pregnancy journey to avoid any genetic abnormality, Down syndrome, or miscarriage. Prenatal screening tests are available to assess the risk of Down syndrome and other chromosomal abnormalities in a developing fetus and are typically offered to pregnant individuals based on their maternal age and medical history.
Genetic abnormalities can play a role in miscarriages, it’s essential to recognize that not all miscarriages are caused by genetic factors. Many factors, including chromosomal abnormalities, hormonal imbalances, and uterine issues, contribute to miscarriage risk. Genetic testing can offer insights into whether genetic abnormalities might contribute to recurrent miscarriages, helping healthcare professionals tailor care and support accordingly.
Genetic testing has revolutionized family planning by providing expectant parents with valuable information about their pregnancy. Non-invasive prenatal testing (NIPT) and diagnostic procedures such as chorionic villus sampling (CVS) and amniocentesis allow for the detection of genetic abnormalities early in pregnancy. This knowledge empowers parents to make informed decisions about their pregnancy journey and potential medical interventions.
Open conversations with healthcare professionals and genetic counselors about genetic abnormalities can help parents understand their options, navigate potential challenges, and make choices aligned with their values and circumstances. When it comes to genetic abnormalities, it’s essential to approach family planning with compassion, families facing challenges deserve empathy and access to accurate information.
Genetic Testing is performed on embryos and designed to detect specific genes that could result in a disease or chromosomal abnormalities that could prevent a pregnancy from progressing.
We at Eve Fertility offer Pre-implantation genetic diagnosis (PGD) and Pre-implantation genetic screening (PGS) testing.
PGD is recommended where there is an identified genetic condition present in one or both of the parents, or if a couple have previously had an affected child. It is possible to test embryos produced in IVF for a specific condition, and only those that are normal are replaced.
PGS is a less specific test, where embryos are checked for chromosomal abnormalities (such as Avoid Down Syndrome and Sick-cell Anemia). PGS may be performed in older women, who have an increased risk of Genetic abnormality, or in cases where recurrent miscarriage have occurred previously.
A genetic abnormality refers to a variation in the DNA sequence, which can lead to health or developmental issues. At Eve fertility clinic, we offer you genetic screening procedures to assess the risk of passing on genetic abnormality to your child, helping you make informed decisions about your fertility journey.
Yes, genetic screening can help you to identify the genetic abnormality called Down syndrome and other chromosomal disorders. Our advanced screening methods enable us to assess the likeliness of such conditions, allowing you to make choices that best suit your family planning goals.
Miscarriage can arise because of diverse factors, which include genetic abnormality. We offer comprehensive genetic testing solutions to identify potential risk factors before conception, reducing the chances of miscarriage. Our team of experts also provides personalized care and guidance throughout your pregnancy journey.
We offer non-invasive prenatal testing (NIPT) to detect genetic abnormality during the earlier stages of pregnancy. This advanced screening method provides accurate information about the health of your baby, helping you make informed decisions about your pregnancy and any necessary interventions.
Preimplantation Genetic Testing (PGT) entails screening embryos for genetic abnormality earlier than they may be implanted through in vitro fertilization (IVF). This technique is beneficial for couples with a history of genetic disorders, recurrent miscarriage, or advanced maternal age, as it increases the chances of a successful pregnancy.
PGD tests embryos for specific genetic abnormality identified in parents and PGS screens embryos for overall chromosomal abnormalities like Down syndrome which is typically recommended for older women. However, choosing the test depends on your medical history and current condition. Consult our doctor today to find suitable treatment plans from our experts.
Yes, it is possible. With PGD and PGS procedures, the embryos that are produced in IVF can be tested for genetic abnormality before implantation.
We at Eve Fertility Center exist to provide you with comprehensive treatment solutions from the initial treatment period to post-treatment care. Thus, we offer our expert genetic counseling services from our professionals for our patients. So that you will become properly aware of the reasons, benefits, and methodologies to avoid Down Syndrome, miscarriage, and other Genetic abnormality.
At Eve Fertility Centre, we are providing you with comprehensive treatment solutions which include genetic counseling, proper guidance of medical interventions, and emotional support along with medical treatments. The parents with positive results for a genetic abnormality or struggling to avoid Down Syndrome and the women who are facing miscarriage strive for these pre counseling and post-treatment care more than medicines which can enhance their treatment outcome.
Yes. Early detection of genetic abnormality can help you to start the medical treatments on time. Also, it will benefit you to make better-informed decisions and manage miscarriage and other health issues during and after pregnancy.
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