Purpose of the Test
- Identify germline mutations in the TP53 gene
- Diagnose Li-Fraumeni Syndrome (LFS)
- Assess the risk of developing various types of cancer
TP53 Genetic Test for Li-Fraumeni | Lahalak Medical Platform
Protect your future and your family through early detection of Li-Fraumeni Syndrome. TP53 testing assesses your risk for multiple primary cancers, enabling a proactive and comprehensive preventive healthcare strategy.
Scientific name: TP53 Gene Mutation Analysis (Li-Fraumeni Syndrome)
A specialized laboratory test to detect germline mutations in the TP53 gene. It diagnoses Li-Fraumeni Syndrome, which increases the risk of breast, bone, and soft tissue cancers, aiding in intensive medical surveillance.
Service type
Genetic laboratory test
Duration
15-20 minutes
Fasting
Fasting is not required
Included Services
- Blood sample collection
- DNA sequencing analysis
- Detailed genetic report
Medical Service Information
Who Should Get Tested?
- Individuals with multiple primary cancers
- People with a strong family history of early-onset cancer
- Patients diagnosed with adrenocortical carcinoma or soft tissue sarcoma
Benefits of Early Detection
- Establishing intensive medical surveillance protocols
- Detecting cancers at early, treatable stages
- Informing family members about their preventive options
Conditions & Notices
- Family medical history is preferred
- Genetic counseling is recommended before testing
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