Reproductive genetic screening can help diagnosis genetic abnormalities, and early detection can often lead to early intervention. Screening for genetic risk factors as early as possible is important. Our screening and diagnostic techniques utilize the most advanced imaging technology available today, including:

Screening Procedures

• Prenatal genetic screening
  We offer prenatal screening for chromosomal abnormalities, such as Down syndrome; neural tube defects, such as spina bifida and other birth defects
  • First-trimester screening through fetal nuchal translucency measurement and maternal serum analysis
  • Integrated first-and second-trimester screening
  • Ultrasound evaluation
     

• Carrier screening based on ancestry
  Individuals from certain ethnic backgrounds have an increased risk for particular genetic conditions. We offer genetic carrier screening for numerous conditions as indicated by a person's ethnic background:
   

  Genetic Condition	Ancestry
  Cystic fibrosis	European, Caucasian
  Hemoglobinopathies (i.e. sickle cell, thalassemia)	Mediterranean, African, Asian
  Ashkenazi Jewish genetic disorder	Eastern European Jewish