Why is this test performed?
- To diagnose Ataxia-Telangiectasia in individuals with movement disorders.
- To assess the hereditary risk of developing specific cancers.
- To screen family members for carrier status of the ATM mutation.
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This genetic screening identifies ATM gene mutations, providing crucial insights into Ataxia-Telangiectasia diagnosis and hereditary cancer risks. It empowers families with the knowledge needed for proactive healthcare and specialized preventative strategies.
Scientific name: Ataxia-Telangiectasia (ATM) Genetic Screening
A molecular test analyzing the ATM gene to diagnose Ataxia-Telangiectasia and assess hereditary predispositions to various cancers, including breast and pancreatic malignancies, ensuring early intervention.
Service type
Genetic Test
Duration
10-15 minutes
Fasting
Fasting is not required
Included Services
- Blood sample collection
- Molecular analysis of ATM gene
- Genetic results report
Medical Service Information
Target Groups
- Individuals with a family history of Ataxia-Telangiectasia.
- Patients diagnosed with early-onset breast or pancreatic cancer.
- Children exhibiting unexplained neurological symptoms or balance issues.
Importance of Results
- Positive results enable intensive surveillance for early cancer detection.
- Assists clinicians in selecting targeted treatments based on genetic profiles.
- Provides essential information for informed family planning decisions.
Conditions & Notices
- Previous medical reports are recommended if available
- Test is not affected by routine medications
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