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Karyotyping Reflex Fish Test – 13, 18, 21, X, Y Amniotic Fluid in Mankhurd

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Overview

Examining chromosomes by karyotyping method in the amniotic fluid, especially chromosomes 13, 18, 21, X, and Y, can help detect congenital abnormalities and identify genetic disorders. FISH (Fluorescence In Situ Hybridization) is conducted when G-banding (karyotyping) analysis fails. This diagnostic test is recommended when there is a need for further investigation into chromosomal abnormalities in prenatal cases. To ensure accurate analysis, the sample submission should include a comprehensive clinical history, including the anomaly scan report. Additionally, a consent form duly signed as per the Pre-Conception and Pre-Natal Diagnostic Techniques (PCPNDT) guidelines must be provided. By combining karyotyping and FISH analysis, healthcare professionals can obtain detailed genetic information, enabling them to identify potential chromosomal anomalies and provide appropriate guidance and support to expectant parents.

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Karyotyping Reflex Fish Test – 13, 18, 21, X, Y Amniotic Fluid Price in Mankhurd

Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Karyotyping Reflex Fish Test – 13, 18, 21, X, Y Amniotic Fluid with a clear pricing structure

The price of Karyotyping Reflex Fish Test – 13, 18, 21, X, Y Amniotic Fluid in Mankhurd is ₹ 11,470

We are committed to deliver accurate and quality results from the best labs in India with complete transparency regarding test cost and turnaround time. No matter where you are, we strive to offer patients high-quality service that is affordable and accessible.

Frequently Asked Questions

To determine the risk for the fetus being born with certain Genetic (chromosomal) abnormalities.

This test is for pregnant women to determine the risk for the fetus being born with certain Genetic (chromosomal) abnormalities.

This test determines the risk for the fetus being born with certain Genetic (chromosomal) abnormalities. FISH for Chromosome 13,18, 21, X and Y is carried out for failed G-banding. Detailed clinical history including anomaly scan report must be submitted with sample. Duly signed consent form as per PCPNDT is must.

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