DNAJB6 Gene Limbgirdle Muscular Dystrophy Autosomal Dominant Type 1E NGS Genetic DNA Test
Introduction
The DNAJB6 Gene Limbgirdle Muscular Dystrophy Autosomal Dominant Type 1E NGS Genetic DNA Test is a sophisticated diagnostic tool designed to identify mutations in the DNAJB6 gene, which are associated with limb-girdle muscular dystrophy. This condition primarily affects muscle strength and function, leading to progressive weakness and disability. Understanding your genetic predisposition is essential for early intervention and informed health decisions.
What the Test Measures
This test detects specific mutations in the DNAJB6 gene that can lead to limb-girdle muscular dystrophy. By analyzing the genetic code, the test helps in confirming a diagnosis or assessing the risk of developing this condition.
Who Should Consider This Test?
Individuals with a family history of limb-girdle muscular dystrophy or those exhibiting symptoms such as muscle weakness, difficulty in movement, or unexplained muscle pain should consider this test. Risk factors include:
- Family history of muscular dystrophy
- Symptoms of muscle weakness or atrophy
- Consultation with a neurologist for further evaluation
Benefits of Taking the Test
- Early diagnosis of potential genetic conditions
- Informed family planning and management options
- Access to specialized care and treatment plans
- Peace of mind through understanding genetic risks
Understanding Your Results
Results from the DNAJB6 Gene test will indicate whether a mutation is present. A positive result may suggest a higher risk of developing limb-girdle muscular dystrophy, while a negative result can provide reassurance. It is important to discuss your results with a healthcare provider for proper interpretation and guidance.
Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| DNAJB6 Gene Limbgirdle Muscular Dystrophy Autosomal Dominant Type 1E NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card. Prior to testing, a genetic counseling session is recommended to draw a pedigree chart of family members affected by the condition.
Book Your Test Today!
We have branches across Kenya, including Nairobi, Mombasa, and Kisumu, and offer home sample collection services. To book your test or for more information, please call or WhatsApp us at +254711564616.
