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Prenatal Diagnosis - Amniotic Fluid, Karyotyping

Karyotyping analyzes the chromosomes in amniotic fluid to detect genetic disorders in a fetus. It helps identify conditions like Down syndrome and other chromosomal abnormalities.

Also known asPrenatal Karyotyping By GTG Banding Prenatal Diagnosis - Amniotic FluidKaryotyping Prenatal Diagnosis - Amniotic FluidKaryotyping

Available via

Home Collection, Lab Visit

Contains

5 parameters

Earliest reports in

12 Working Days

Test details

Prenatal Diagnosis - Amniotic Fluid, Karyotyping Test in Gorakhpur Overview

Preparations

No special preparations needed

Test included
Prenatal Diagnosis - Amniotic Fluid, Karyotyping includes 5 parameters

  • Specimen
  • Indications
  • Cells Counted & Analysed
  • Cells Karyotyped
  • Karyotype
Frequently Asked Questions

This genetic test analyzes the chromosomes present in fetal cells obtained from the amniotic fluid to detect chromosomal abnormalities such as Down syndrome, Turner syndrome, and other genetic disorders.

It is recommended for pregnant women at higher risk of chromosomal abnormalities due to advanced maternal age, a history of genetic disorders, or abnormal prenatal screening results.

A procedure called amniocentesis is performed, where a small amount of amniotic fluid is extracted from the womb using a thin needle. The fetal cells in the fluid are then cultured and analyzed under a microscope to examine their chromosomal structure.

A normal result means the fetus has the expected number of chromosomes without structural abnormalities. An abnormal result may indicate genetic disorders, which require further consultation with a genetic counselor or specialist to discuss possible outcomes and management options.

Amniocentesis carries a small risk of complications such as infection, bleeding, or miscarriage. The decision to undergo this test should be made after discussing the benefits and risks with a healthcare provider.

Test code

5832K

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Amniotic FluidPlain Sterile Vaccutainer 15 ML

Specimen stability information

Amniotic Fluid

Collection instructions

Aminotic Fluid + Duly Filled Amniotic Fliud Trf + Clinical History. Consent Form - G With Pnd Registration Number Mandatory. Specimen Should Reach Us In 24 Hrs After Collection In Sterile Condition.

Specimen rejection criteria

Test run frequency

Every Day TIME - 07:00

Turn around time

12 Working Days

Performing locations

Department

  • Cytogenetics

CPT and Loinc codes

Prenatal Diagnosis - Amniotic Fluid, Karyotyping

₹12000

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