Common Genetic Disorders Detected Through Prenatal Screening

Prenatal genetic screening can give parents-to-be valuable insights into their baby’s health early in pregnancy. By identifying conditions like Down Syndrome and cystic fibrosis, these screenings help families feel more prepared and confident about what lies ahead. Early detection means parents can make informed decisions and plan for the care their baby might need. With today’s advancements, these tests are more accurate and accessible, providing peace of mind during a special time.

At Chedid Grieco, we’re here to guide you with personalized care through every step of your fertility journey. With 30 years of experience and nearly 9,000 babies born through our treatments, we’re proud to support all types of families, including LGBTQI+ couples. Our consultations are held in Miami, and treatments take place at our clinic in Brazil, which is fully licensed by the Food and Drug Administration and New York Department of Health.

Conditions That Can Be Detected Through Prenatal Screening

Prenatal genetic screening can help identify a variety of genetic and chromosomal conditions early in pregnancy. These tests provide parents with critical information, allowing them to prepare for any special medical needs their child may have. Below are some of the most common conditions detected through prenatal screening.

Down Syndrome (Trisomy 21)

Down syndrome is one of the most commonly detected conditions through prenatal screening. It is caused by the presence of an extra 21st chromosome and can lead to developmental delays and intellectual disabilities. Screening for Down syndrome is typically offered to all pregnant women, and early detection allows families to plan for any necessary support or interventions.

Edwards Syndrome (Trisomy 18)

Edwards syndrome occurs when a baby has an additional 18th chromosome. It’s a more severe condition than Down syndrome, often leading to significant developmental issues and a shorter life expectancy. Prenatal screening can help identify this condition early, allowing parents to make informed decisions about the pregnancy and potential medical care.

Patau Syndrome (Trisomy 13)

Patau syndrome is a rare but serious genetic disorder caused by an extra chromosome. It can lead to severe intellectual disabilities, physical abnormalities, and a reduced life expectancy. Detecting this condition early through prenatal screening allows parents to be better prepared for the care their baby may need after birth.

Cystic Fibrosis

Cystic fibrosis is a genetic disorder that affects the lungs and digestive system. It is caused by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein and can be detected through carrier screening or targeted prenatal testing. While there is no cure for cystic fibrosis, early detection gives families the chance to prepare for specialized care and treatment options.

Sickle Cell Disease

Sickle cell disease is a hereditary blood disorder that affects the shape of red blood cells, causing them to form a sickle shape. This condition can lead to pain, infections, and other health issues. Prenatal screening can detect sickle cell disease if both parents are carriers of the gene, allowing families to plan for potential medical needs early on.

Spina Bifida

Although it is not a genetic disorder, Spina Bifida is a birth defect of the spine that can also be detected through prenatal screening. It occurs when the spinal column does not close completely during early development. Early detection allows parents to explore treatment options and prepare for the specialized care their child may require.

These screenings provide valuable insights into your baby’s health so you can make well-informed decisions about your and your baby’s health.

Why Choose Chedid Grieco for Prenatal Genetic Screening

At Chedid Grieco, we are committed to providing the highest level of personalized care during your pregnancy journey. With over 30 years of experience and nearly 9,000 successful births, we understand the importance of early detection in ensuring your baby’s health. Our advanced prenatal screening options allow families to feel informed and confident as they prepare for their child’s future. Whether you’re concerned about common genetic conditions or seeking peace of mind, we are here to guide you every step of the way.

Our clinic proudly serves a diverse range of families, including LGBTQI+ couples, offering tailored care that meets your specific needs. Consultations are conveniently held in Miami, and treatments take place at our state-of-the-art, FDA and NYDH-licensed clinic in Brazil. To take the next step in your fertility journey, reach out to us via our contact form or learn more about our fertility tourism page. You can also call us at (305) 912-0050.