PRENATAL DIAGNOSIS-AMNIOTIC FLUID (FISH+KARYO)

This combined test uses both karyotyping and FISH to detect chromosomal abnormalities in amniotic fluid. It provides a comprehensive diagnosis of potential genetic conditions in a fetus.

Also known asPrenatal Diagnosis-amniotic Fluid (karyotype + Fish) Prenatal Diagnosis-amniotic Fluid (karyotype + Fish)

Available via

Home Collection, Lab Visit

Contains

14 parameters

Earliest reports in

18 Working Days

Test details
Preparations

No special preparations needed

Test included
PRENATAL DIAGNOSIS-AMNIOTIC FLUID (FISH+KARYO) includes 14 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

  • Specimen
  • Indications
  • Cells Counted & Analysed
  • Cells Karyotyped
  • Karyotype

Test code

5832

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Amniotic FluidPlain Sterile Vaccutainer 35 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

'

Turn around time

18 Working Days

Performing locations

Department

  • Cytogenetics

CPT and Loinc codes

PRENATAL DIAGNOSIS-AMNIOTIC FLUID (FISH+KARYO)

18000