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Requisites
Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

  • Test Name: Deletion 20Q Test By FISH
  • Maximum Days for Report: 14 days

What are the prerequisites for the test Deletion 20Q Test By FISH

Prerequisites for the Deletion 20Q Test By FISH:

  1. Specimen: A fresh, unfixed tumor tissue sample is required for the test.
  2. Test Request Form: The appropriate test request form must be completed and submitted along with the specimen.
  3. Clinical Information: Relevant clinical information about the patient, including medical history and any previous test results, should be provided.
  4. Consent: Informed consent from the patient or legal guardian is necessary before the test can be performed.
  5. Proper Storage: The specimen should be properly handled and stored according to the specific instructions provided by the testing laboratory.

What are the measure values for the test Deletion 20Q Test By FISH

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What does this test Deletion 20Q Test By FISH identify?

Deletion 20Q Test By FISH

  • This test identifies deletions in DNA using Fluorescence In Situ Hybridization (FISH) technology.
  • Deletions are genetic abnormalities where a portion of the DNA is missing.
  • By analyzing specific regions of the DNA with FISH probes, this test can detect deletions in chromosomes.
  • Deletions can be associated with various genetic disorders and diseases.
  • Results from this test can provide valuable information for diagnosis, prognosis, and treatment planning.

Why is this test Deletion 20Q Test By FISH taken?

Reason for Taking Deletion 20Q Test By FISH

Reason for Taking Deletion 20Q Test By FISH

The Deletion 20Q Test By FISH is typically taken to detect any chromosomal abnormalities, specifically deletions, using fluorescence in situ hybridization (FISH) technology. This test is often used in clinical settings to diagnose genetic disorders such as DiGeorge syndrome, Prader-Willi syndrome, and Angelman syndrome.

By analyzing specific regions of chromosomes for deletions, the test can provide valuable information about a patient's genetic makeup and help healthcare providers make informed decisions regarding treatment and management of genetic conditions.

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