When is Trisomy (Aneuploidy) for Chromosome 13 & 21 By FISH Amniotic Fluid recommended, and who should take the test?

This test is recommended for pregnant women who have a higher risk of having a baby with chromosomal abnormalities due to factors like advanced maternal age or abnormal results from other prenatal screenings. It is also recommended for women with a family history of genetic disorders.

What to expect during the Trisomy (Aneuploidy) for Chromosome 13 & 21 By FISH Amniotic Fluid?

During the test: • A sample of amniotic fluid will be collected using a sterile falcon centrifuge tube. • The sample will be sent to the laboratory for analysis using the FISH method.

What preparations are required before the Trisomy (Aneuploidy) for Chromosome 13 & 21 By FISH Amniotic Fluid?

Before the test: • Detailed clinical history, including anomaly scan report, must be submitted with the sample. • A duly signed consent form as per PCPNDT must be provided. • Follow any specific instructions provided by your doctor regarding fasting or medication. Please reach out to your healthcare provider for any specific requirements.

What other tests may be ordered with Trisomy (Aneuploidy) for Chromosome 13 & 21 By FISH Amniotic Fluid?

Additional tests that may be ordered alongside this test include: • First trimester screening: A combination of blood tests and ultrasound to assess the risk of chromosomal abnormalities • Level II ultrasound: A detailed ultrasound examination to detect any structural abnormalities in the foetus • Cell-free DNA testing: A blood test that screens for certain chromosomal abnormalities in high-risk pregnancies

What is Down syndrome?

Down syndrome is a genetic disorder caused by the presence of an extra copy of chromosome 21. It leads to physical and intellectual disabilities. It is the most common chromosomal abnormality detected in babies, occurring in approximately 1 in 800 births in India.

Trisomy (Aneuploidy) for Chromosome 13 & 21 By FISH Amniotic Fluid in Hyderabad

Also known as: Trisomy (Aneuploidy) for Chromosome (13 & 21), Amniotic Fluid

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Overview

The Trisomy (Aneuploidy) FISH test is performed on amniotic fluid samples to detect aneuploidies specifically in chromosomes 13 and 21 using Fluorescence In Situ Hybridization. This diagnostic test is crucial for prenatal screening and diagnosis, aiding in the identification of conditions such as Down syndrome (Trisomy 21) and Patau syndrome (Trisomy 13). To ensure accurate analysis, it is important to submit a detailed clinical history, including the anomaly scan report, along with the sample. Additionally, a consent form in accordance with the Pre-Conception and Pre-Natal Diagnostic Techniques (PCPNDT) guidelines must be duly signed and provided. The Trisomy FISH test offers valuable information to expectant parents and healthcare professionals, allowing for informed decisions, appropriate counseling, and support in managing pregnancies involving these chromosomal abnormalities.

Trisomy (Aneuploidy) for Chromosome (13 & 21), Amniotic Fluid Price in Hyderabad

Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Trisomy (Aneuploidy) for Chromosome (13 & 21), Amniotic Fluid with a clear pricing structure

The price of Trisomy (Aneuploidy) for Chromosome (13 & 21), Amniotic Fluid in Hyderabad is ₹ 4,900

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.

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