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Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

The maximum days the report can be obtained for the test Karyotyping (KT)- Prenatal test is typically 10-14 days from the date of sample collection.

What are the prerequisites for the test Karyotyping (KT)- Prenatal test

  • Written consent from the patient or legal guardian
  • Confirmation of pregnancy
  • Availability of fetal tissue (amniotic fluid, chorionic villi, or fetal blood)
  • Properly labeled and documented samples
  • Confirmation of gestational age
  • Discussion of risks and benefits of the test with the patient

What are the measure values for the test Karyotyping (KT)- Prenatal test

  • Test name: Karyotyping (KT) - Prenatal
  • Normal result: 46 chromosomes present, no abnormalities detected
  • Abnormal results may include: Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), Trisomy 13 (Patau syndrome), sex chromosome abnormalities
  • Additional information: Karyotyping can also detect structural abnormalities in chromosomes

What does this test Karyotyping (KT)- Prenatal test identify?

  • Karyotyping (KT) - Prenatal test identifies any chromosomal abnormalities in a fetus.
  • It can detect conditions such as Down syndrome, Turner syndrome, and trisomy 18.
  • The test involves analyzing the number, size, and shape of the chromosomes in a sample of amniotic fluid or placental tissue.
  • Results from the test can help determine the risk of genetic disorders in the fetus and guide medical decisions during pregnancy.

Why is this test Karyotyping (KT)- Prenatal test taken?

Karyotyping (KT) - Prenatal test is taken to analyze the chromosomes of an unborn baby during pregnancy. This test is usually recommended when there are concerns about genetic disorders or abnormalities in the fetus. Karyotyping can detect chromosomal abnormalities such as Down syndrome, Turner syndrome, and trisomy 18, among others.

The test involves obtaining a sample of amniotic fluid or tissue from the placenta through procedures like amniocentesis or chorionic villus sampling. These samples are then cultured and the chromosomes are analyzed to check for any abnormalities in their number or structure.

By identifying any chromosomal abnormalities early on in the pregnancy, parents and healthcare providers can make informed decisions about the future care and management of the baby. This test can provide valuable information about the baby's health and development, helping parents prepare for any potential challenges that may arise.

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