Fluorescence In Situ Hybridization

FISH is a sensitive method for detecting chromosomal abnormalities, particularly effective for identifying common aneuploidies in uncultured amniocytes within 24-48 hours.

Fluorescence in Situ Hybridization (FISH Test)

FISH is a sensitive method for detecting chromosomal abnormalities, particularly effective for identifying common aneuploidies (abnormal numbers of chromosomes) in uncultured amniocytes within 24-48 hours. It complements routine chromosome analysis but should be used with more than just diagnosing common aneuploidy conditions.

Purpose:

FISH rapidly tests the number of selected chromosomes in the placenta, amniotic fluid, or fetal blood samples, providing diagnostic and prognostic information. Results are confirmed with karyotyping or microarray analysis.

When it is done : 16 weeks of pregnancy onwards

Tested Chromosomes:

The standard set includes chromosomes 13, 18, 21, X, and Y. Additional probes can be requested for specific conditions (e.g., 22q11.2 deletion syndrome).

Specimen Collection:

Samples are obtained from:

Report Time:

Results are typically available within 3-4 working days.

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Expertise and Care: Our highly skilled radiologists bring years of experience, ensuring your scan is performed with the utmost precision and care.
Advanced Technology: We use cutting-edge ultrasound equipment that provides high-resolution images for accurate diagnoses and enhances your comfort during the procedure.
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Transparency and Respect: We believe in transparency. You have the right to understand how your health information is used, and we ensure your confidentiality is always respected.
Comprehensive Care: Our dedicated team prioritizes your health and well-being, offering a seamless and comfortable scanning experience you can trust.

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Fluorescence In Situ Hybridization