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Chromosome Analysis Amniocentesis Karyotyping Amniotic Fluid

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Chromosome Analysis Amniocentesis Karyotyping Amniotic Fluid

What is this test?

Amniocentesis is usally performed between 15 and 18 weeks of gestation to rule out chromosome abnormalities such as trisomies, deletions, translocations etc. Study can also be performed during later part of the pregnancy. The most common indications for chromosome analysis for prenatal diagnosis are AMA- advance maternal age, abnormal serum alphafetoprotein, abnormal first trimester or quad screen, abnormal noninvasive prenatal screening, family history of chromosome abnormality, abnormal fetal ultrasound, previous child with chromosome abnormality, parental anxiety. The specimen can also be used for additional studies such as Prenatal Aneuploidy Detection using Fluorescence in situ hybridization - FISH study.

What is the preparation needed for doing this test?

No special preparation is needed for Chromosome Analysis Amniocentesis Karyotyping Amniotic Fluid. Inform your doctor if you are on any medications or have any underlying medical conditions or allergies before undergoing Chromosome Analysis Amniocentesis Karyotyping Amniotic Fluid. Your doctor depending on your condition will give specific instructions.

What are the normal values of results of this test?

GenderAge groupsValue
UNISEXAll age groupsResults depend on the type of chromosomal anomaly/ abnormality

Test Price

4600 - ₹12000

Average price range of the test depends on factors like city, quality and availability.

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