RXYLT1 Gene Muscular Dystrophy-Dystroglycanopathy Congenital with Brain and Eye Anomalies Type A10 NGS Genetic DNA Test
Introduction
The RXYLT1 Gene Muscular Dystrophy-Dystroglycanopathy Congenital with Brain and Eye Anomalies Type A10 NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic mutations that may lead to severe neurological disorders. This test employs Next Generation Sequencing (NGS) technology to provide precise insights into the genetic underpinnings of muscular dystrophy and associated conditions.
What the Test Measures
This genetic test specifically measures mutations in the RXYLT1 gene, which are linked to dystroglycanopathy, a condition that can lead to muscular dystrophy and various brain and eye anomalies. By detecting these mutations, healthcare providers can better understand the underlying causes of the patient’s symptoms.
Who Should Consider This Test
Individuals who exhibit symptoms of muscular dystrophy, such as muscle weakness, difficulty in movement, or developmental delays, should consider this test. Additionally, those with a family history of dystroglycanopathy or related neurological disorders may benefit from genetic testing to assess their risk.
Benefits of Taking the Test
- Accurate diagnosis of genetic conditions related to muscular dystrophy.
- Guidance for treatment options based on genetic findings.
- Informed family planning decisions through genetic counseling.
- Access to appropriate medical care and support services.
Understanding Your Results
Results from the RXYLT1 Gene Muscular Dystrophy-Dystroglycanopathy test will provide insights into the presence of specific mutations. A genetic counselor will help interpret these results, discussing their implications for the patient and their family.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| RXYLT1 Gene Muscular Dystrophy-Dystroglycanopathy Congenital with Brain and Eye Anomalies Type A10 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Availability and Booking
We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu, providing convenient access to this essential genetic test. We also offer a home sample collection service for your convenience.
To book the RXYLT1 Gene Muscular Dystrophy-Dystroglycanopathy test or for more information, please call or WhatsApp us at +254713408028.
Your health is our priority, and we are here to support you every step of the way.
