Prenatal Diagnosis - Amniotic Fluid, FISH

Available viaHome Collection, Lab Visit
GenderFemale
Contains9 parameters
Earliest reports in5 Working Days
PreparationNo preparation needed

Overview of Prenatal Diagnosis - Amniotic Fluid, FISH in Thane

The Prenatal Diagnosis – Amniotic Fluid, FISH Test is a specialized genetic test performed on an amniotic fluid sample to rapidly detect certain chromosomal abnormalities in a developing fetus. It uses Fluorescence In Situ Hybridization (FISH) technology to identify changes in selected chromosomes that may be associated with genetic conditions. This test is often recommended when there is an increased risk of chromosomal abnormalities based on maternal age, prenatal screening results, ultrasound findings, or family history. It provides valuable information to support prenatal evaluation and clinical decision-making.

Who Should Get This Test Done?

This test may be recommended for individuals who:

●     Have abnormal findings on prenatal screening or ultrasound examinations.

●     Are at an increased risk of fetal chromosomal abnormalities due to maternal age or medical history.

●     Have a family history of genetic or chromosomal disorders requiring further prenatal evaluation.

●     Need additional genetic assessment following a healthcare provider’s recommendation.

●     Wish to investigate the possibility of specific chromosomal conditions during pregnancy after appropriate genetic counselling.

Why Consider This Test?

Pregnancy can sometimes raise questions that routine screening tests cannot fully answer. The Prenatal Diagnosis – Amniotic Fluid, FISH Test offers a focused genetic assessment by detecting selected chromosomal abnormalities in fetal cells. It serves as an important follow-up test when there is a higher likelihood of genetic conditions, helping healthcare providers and expectant parents gain additional information for informed pregnancy management and future care planning.

More Information

This test is performed on fetal cells obtained from an amniotic fluid sample and uses fluorescent DNA probes that bind to specific chromosomes. It is commonly used to evaluate chromosomes that are most frequently associated with major chromosomal disorders. While the FISH test provides targeted genetic information, it is often used alongside other prenatal diagnostic tests and clinical findings to achieve a comprehensive assessment of fetal health.

Other Names

●     Prenatal FISH Test – Amniotic Fluid

●     Amniotic Fluid FISH Analysis

●     Fetal Aneuploidy FISH Test

●     Fluorescence In Situ Hybridization (FISH), Amniotic Fluid

●     Prenatal Chromosomal FISH Test

Test included

Prenatal Diagnosis - Amniotic Fluid, FISH includes 9 parameters

  • Clinical Indications
  • 1st Hybridization (green Chr 13)
  • 1st Hybridization (orange Chr 21)
  • Total Number Of Cells Analyzed
  • Interpretation
  • 2nd Hybridization (aqua Chr 18)
  • 2nd Hybridization (sex Chromosomes)
  • Total Number Of Cells Analysed
  • Interpretation

Test code

5832F

CPT and Loinc codes

Department

  • Cytogenetics

Turn around time

5 Working Days

Test run frequency

Every Day TIME - 07:00

Performing locations

2 labs across India

Specimen vol. and vacutainer information

SpecimenVacutainerVolume
Amniotic FluidPlain Sterile Vaccutainer 10 ML

Specimen stability information

Amniotic Fluid

Collection instructions

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

Prenatal Diagnosis - Amniotic Fluid, FISH

8560

Health Checkup Category

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Complete Care Packages

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