Purpose of the Test
- Identify mutations in the PTEN gene responsible for Cowden syndrome.
- Assess the risks of developing various hereditary malignancies.
- Provide accurate information for relatives regarding genetic inheritance.
Book PTEN Genetic Test in Saudi Arabia | Lahalak Medical Platform
Identify cancer risks early with advanced PTEN genetic testing. This precise assessment detects hereditary predispositions to Cowden syndrome, empowering you and your family to take proactive, life-saving preventive measures.
Scientific name: Cowden Syndrome Genetic Mutation Assessment (PTEN)
An advanced laboratory test to detect PTEN gene mutations associated with Cowden syndrome. It assesses risks for breast, thyroid, and endometrial cancers, ensuring early preventive care and personalized medical surveillance.
Service type
Laboratory test
Duration
15-20 minutes
Fasting
Fasting is not required
Included Services
- Blood sample collection
- PTEN gene sequencing
- Medical results report
Medical Service Information
Target Groups
- Individuals with a family history of early-onset breast or thyroid cancer.
- Patients presenting with multiple benign growths (Hamartomas).
- Individuals whose first-degree relatives have a confirmed PTEN mutation.
Clinical Significance
- Positive results guide the implementation of intensive screening programs.
- Informs decisions regarding prophylactic surgeries if necessary.
- Improves early detection rates for syndrome-associated cancers.
Conditions & Notices
- Family medical history is recommended
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