GLB1 Gene Mucopolysaccharidosis Type 4B NGS Genetic DNA Test
Introduction to the Test
The GLB1 Gene Mucopolysaccharidosis Type 4B NGS Genetic DNA Test is a cutting-edge diagnostic tool used to identify mutations in the GLB1 gene, which are responsible for Mucopolysaccharidosis Type 4B (MPS IVB). This condition is a rare metabolic disorder that can lead to serious health issues if left undiagnosed and untreated. Understanding your genetic predisposition is crucial for effective management and treatment planning.
What the Test Measures
This test detects specific genetic mutations in the GLB1 gene using Next Generation Sequencing (NGS) technology. By analyzing the DNA, healthcare providers can determine if an individual is at risk for developing MPS IVB, which affects various bodily systems and can lead to progressive health complications.
Who Should Consider This Test?
- Individuals exhibiting symptoms such as skeletal abnormalities, short stature, or joint stiffness.
- Those with a family history of Mucopolysaccharidosis Type 4B.
- Patients experiencing unexplained developmental delays or organ dysfunction.
Benefits of Taking the Test
- Early detection of genetic disorders can lead to timely interventions.
- Provides crucial information for family planning and genetic counseling.
- Helps in understanding potential health risks associated with MPS IVB.
Understanding Your Results
Results from the GLB1 Gene Mucopolysaccharidosis Type 4B NGS Genetic DNA Test generally take 3 to 4 weeks. Our healthcare professionals will guide you through the results, explaining what they mean for your health and any necessary next steps.
Test Pricing
| Price Type | Amount (KSh) |
|---|---|
| Discount Price | 40000 |
| Regular Price | 56000 |
Book Your Test Today!
We have branches across Kenya, including Nairobi, Mombasa, and Kisumu, and we also offer home sample collection services for your convenience. To book the GLB1 Gene Mucopolysaccharidosis Type 4B NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
Pre-Test Instructions
Before taking the test, it is essential to have a clinical history assessment and a genetic counseling session to draw a pedigree chart of family members affected by Mucopolysaccharidosis Type 4B.
