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IMR/CaRC/HAEM/22/2203/03(1)/REQFormDNA ANALYSIS FOR THALASSAEMIA SYNDROMES & HAEMOGLOBINOPATHIESFor IMR/ HKL/ HSB used only Type of specimen blood DNA othersPlease below, WHERE you wish to send the
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How to fill out dna analysis for thalassaemia

01
Obtain a DNA sample through blood or saliva collection.
02
Complete the consent form indicating permission for DNA analysis.
03
Provide relevant medical history, including family history of thalassaemia.
04
Label the sample with your details, including name, date of birth, and date of collection.
05
Send the sample to a certified laboratory for analysis.
06
Wait for results, which may take a few weeks, and follow up with your healthcare provider.

Who needs dna analysis for thalassaemia?

01
Individuals with a family history of thalassaemia.
02
Pregnant women who may be carriers of thalassaemia genes.
03
Couples planning to have children, especially if one or both partners are carriers.
04
Individuals showing symptoms of thalassaemia such as anemia or fatigue.
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DNA analysis for thalassaemia is a genetic test that identifies mutations in genes associated with thalassaemia disorders, helping to determine if an individual is a carrier or affected by the condition.
Individuals who are at risk of having thalassaemia, such as those with a family history of the disorder or belonging to high-risk ethnic groups, may be required to file DNA analysis. Additionally, couples planning to have children might be advised to undergo this testing.
To fill out DNA analysis for thalassaemia, individuals should complete a consent form that includes personal information, family medical history, and any previous blood test results. This form should then be submitted to a certified genetic testing laboratory.
The purpose of DNA analysis for thalassaemia is to diagnose the disorder, assess carrier status, guide treatment options, and provide information for family planning.
The information that must be reported includes the specific genetic mutations identified, the carrier status of the individual, and any recommendations for further testing or medical management.
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