Lab test

FISH - MDS Panel - Chromosomes 5Q, 7Q, 8Q & 20Q

The FISH – MDS Panel Test is a genetic test used to detect chromosomal abnormalities associated with myelodysplastic syndromes (MDS).
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ReportWithin 24 hrs
SampleBlood
CollectionHome or centre
FastingNot needed
How it works
1
Book in a minute
Add to cart, pick a date and time slot, pay online or at collection.
2
Sample collected at home or centre
A trained phlebotomist arrives in your slot with sealed, single-use kits.
3
Report on WhatsApp
Within 24 hours on WhatsApp and under My Orders.
Parameters covered4 parameters
Chromosome 5q Deletion
Chromosome 7q Deletion
Chromosome 8q Abnormality
Chromosome 20q Deletion
Preparation
No special preparation needed unless your doctor advises otherwise.
About this test

The FISH – MDS Panel Test is a genetic test used to detect chromosomal abnormalities associated with myelodysplastic syndromes (MDS).

FISH - MDS PANEL - CHROMOSOMES 5Q, 7Q, 8Q & 20Q

This Test is a specialized molecular cytogenetic test that uses Fluorescence In Situ Hybridization (FISH) to detect specific chromosomal abnormalities.

This test focuses on common genetic changes involving chromosomes 5q, 7q, 8q, and 20q, which are frequently associated with myelodysplastic syndromes (MDS) and other bone marrow disorders. Identifying these abnormalities helps in diagnosis, prognosis, and treatment planning.

The purpose of the test is to:

  • Detect chromosomal abnormalities linked to MDS
  • Identify deletions or changes in chromosomes 5q, 7q, 8q, and 20q
  • Support diagnosis of bone marrow disorders
  • Assist in prognosis and treatment planning

FISH - MDS PANEL - CHROMOSOMES 5Q, 7Q, 8Q & 20Q Test

The FISH – MDS Panel is a genetic laboratory test used to detect specific chromosomal abnormalities associated with myelodysplastic syndromes (MDS). FISH (Fluorescence In Situ Hybridization) uses fluorescent DNA probes to identify changes in specific chromosome regions.

This panel commonly evaluates abnormalities involving 5q, 7q, 8q, and 20q, which can occur in patients with MDS and other myeloid disorders. Detecting these abnormalities can provide additional information for diagnosis, classification, prognosis, and treatment planning.

The test is generally interpreted along with CBC results, peripheral blood smear, bone marrow examination, morphology, cytogenetic studies, and other molecular tests. A normal FISH result does not completely exclude MDS because not all genetic abnormalities are detected by this particular panel.

This Test is Recommended for Individuals:

  • Individuals with suspected myelodysplastic syndrome (MDS)
  • Patients with persistent or unexplained abnormalities in blood cell counts
  • Individuals with unexplained anemia, low platelets, or low white blood cell counts
  • Patients undergoing evaluation of abnormal bone marrow findings
  • Individuals requiring chromosomal assessment for suspected myeloid neoplasms
  • Patients with an established MDS diagnosis requiring additional genetic or prognostic information
  • Individuals undergoing evaluation or monitoring as advised by a hematologist

FAQs

1. What does the MDS FISH Panel detect?
It detects specific chromosomal abnormalities involving regions of 5q, 7q, 8q and 20q that may be associated with myelodysplastic syndromes and other myeloid disorders.

2. Does an abnormal FISH result confirm MDS?
Not necessarily. A detected chromosomal abnormality can support the diagnosis, but MDS diagnosis requires correlation with blood counts, bone marrow morphology, clinical findings, and other genetic or cytogenetic investigations.

3. Does a normal MDS FISH result rule out myelodysplastic syndrome?
No. The panel examines only selected chromosome regions. Other genetic or chromosomal abnormalities may be present even when this FISH panel is negative, so additional investigations may be recommended when clinical suspicion remains high.

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Questions people ask
How soon will I get my report?
Your report is delivered within 24 hours of sample collection — on WhatsApp and under My Orders.
Is home sample collection available?
Yes. A trained phlebotomist visits your home with sealed, single-use kits. Home collection is free.
Do I need to fast or prepare?
No fasting is required for this test unless your doctor advises otherwise.
How do I pay?
Pay online (UPI / cards) or pay at collection or at the centre. The price you see is what you pay — it includes the report, with no hidden charges.
Is the lab accredited?
Yes. Prima Diagnostics runs NABL-certified labs with strict quality control across 7 centres in Bengaluru.