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Prenatal Screening Tests
Early Screening for a Healthier Pregnancy

At Sakkthi Clinical Laboratory & Andrology Centre, we provide prenatal screening tests using reliable laboratory methods and advanced diagnostic techniques. Our laboratory supports doctors and expecting parents by delivering accurate screening results that help monitor the health and development of the baby during pregnancy.

What are Prenatal Screening Tests?

Prenatal screening tests are tests performed during pregnancy to assess the risk of certain genetic conditions or developmental abnormalities in the baby. These tests help identify potential concerns early so that doctors can recommend further evaluation or appropriate care if necessary.

Who Needs Prenatal Screening Tests?
  • All Pregnant Women as part of routine pregnancy care

  • Women aged 35 years or above who may have higher genetic risk

  • Couples with a family history of genetic disorders

  • Women with previous pregnancy complications or birth defects

  • Pregnancies where doctors recommend additional fetal health monitoring

First Trimester Screening
  • Performed during 11 to 13 weeks of pregnancy

  • Includes blood tests and ultrasound scan (NT scan)

  • Helps assess the risk of chromosomal conditions such as Down syndrome

  • Evaluates certain pregnancy-related markers in maternal blood

  • Provides early information about fetal health


Second Trimester Screening
  • Usually performed during 15 to 20 weeks of pregnancy

  • Includes blood tests often known as triple or quadruple marker screening

  • Helps assess the risk of chromosomal abnormalities and neural tube defects

  • Provides additional information about fetal development


Advanced Prenatal Genetic Testing
  • Uses advanced genetic testing methods to evaluate fetal genetic material

  • Helps detect chromosomal abnormalities with higher accuracy

  • Often recommended for high-risk pregnancies or when screening results require further evaluation

  • Provides more detailed information about fetal genetic health

First Trimester Screening
  • Performed during 11 to 13 weeks of pregnancy

  • Includes blood tests and ultrasound scan (NT scan)

  • Helps assess the risk of chromosomal conditions such as Down syndrome

  • Evaluates certain pregnancy-related markers in maternal blood

  • Provides early information about fetal health

Second Trimester Screening
  • Usually performed during 15 to 20 weeks of pregnancy

  • Includes blood tests often known as triple or quadruple marker screening

  • Helps assess the risk of chromosomal abnormalities and neural tube defects

  • Provides additional information about fetal development

Advanced Prenatal Genetic Testing
  • Uses advanced genetic testing methods to evaluate fetal genetic material

  • Helps detect chromosomal abnormalities with higher accuracy

  • Often recommended for high-risk pregnancies or when screening results require further evaluation

  • Provides more detailed information about fetal genetic health