Purpose of the Test
- Confirm clinical diagnosis of retinoblastoma
- Distinguish between hereditary and non-hereditary forms
- Enable early screening for siblings and close relatives
Book RB1 Genetic Test | Lahalak Medical Platform
An advanced genetic test to detect mutations in the RB1 gene, enabling early diagnosis of retinoblastoma in children and assessing hereditary risks for relatives to ensure timely medical intervention.
Scientific name: Retinoblastoma Genetic Sequencing (RB1 Gene)
A precise laboratory test analyzing DNA for mutations in the RB1 gene linked to retinoblastoma. It evaluates hereditary risks and assists in developing comprehensive therapeutic and preventive plans.
Service type
Genetic laboratory test
Duration
15-20 minutes
Fasting
Fasting is not required
Included Services
- Blood sample collection
- Genetic sequencing analysis
- Detailed medical report
Medical Service Information
Target Groups
- Children newly diagnosed with retinoblastoma
- Individuals with a known family history of the disease
- Parents seeking to assess risk for future offspring
Clinical Significance
- Guides the frequency of ophthalmological monitoring
- Avoids unnecessary clinical exams for non-carrier relatives
- Assists in personalized treatment planning based on mutation type
Conditions & Notices
- Previous medical reports preferred
- Genetic counseling recommended before test
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