DNA Labs UAE is at the forefront of genetic testing and analysis, providing comprehensive services to diagnose and understand various genetic disorders. Among the numerous tests offered, one significant test focuses on the FKTN gene, which is associated with Limb-girdle muscular dystrophy autosomal recessive type 2M (LGMDR2, formerly LGMD2M). This article delves into the symptoms of this condition, the importance of genetic testing, and details about the FKTN gene test, including its cost.
Symptoms of FKTN Gene Limb-girdle Muscular Dystrophy Autosomal Recessive Type 2M
Limb-girdle muscular dystrophy type 2M is a form of muscular dystrophy that affects the voluntary muscles around the hips and shoulders (the limb-girdle muscles). The symptoms typically begin in childhood and can vary in severity. Common symptoms include:
- Difficulty walking or running, which may progress to difficulty standing
- Muscle weakness in the shoulders, arms, hips, and legs
- Increased difficulty with tasks requiring upper body strength
- Stiff or tight muscles (contractures) in the legs
- Progressive loss of muscle mass (muscle wasting)
As the disease progresses, individuals may require the use of mobility aids, such as braces, walkers, or wheelchairs. Early diagnosis and intervention are crucial in managing the symptoms and improving the quality of life for those affected.
The Importance of Genetic Testing for FKTN Gene Limb-girdle Muscular Dystrophy
Genetic testing plays a pivotal role in diagnosing limb-girdle muscular dystrophy type 2M. By analyzing the FKTN gene, specialists can confirm the diagnosis, which is essential for planning treatment, understanding the progression of the disease, and providing genetic counseling to families. The FKTN gene test is a targeted examination that looks for mutations known to cause the condition. Identifying the specific mutation can also help in understanding the potential severity of the disease and in some cases, can inform treatment decisions.
FKTN Gene Limb-girdle Muscular Dystrophy Autosomal Recessive Type 2M Genetic Test at DNA Labs UAE
DNA Labs UAE offers the FKTN gene test for diagnosing limb-girdle muscular dystrophy type 2M. The test is conducted with the highest standards of accuracy and confidentiality, ensuring reliable results for patients and their families. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for mutations in the FKTN gene.
The cost of the FKTN gene test at DNA Labs UAE is 4400 AED. This price includes the full cost of the test, from sample collection to the delivery of results. Patients and families interested in undergoing the test or learning more about it can find additional information and initiate the testing process through the following link: FKTN Gene Test Information.
Conclusion
Limb-girdle muscular dystrophy autosomal recessive type 2M is a challenging condition that significantly impacts the lives of those affected and their families. Early diagnosis through genetic testing, such as the FKTN gene test offered by DNA Labs UAE, is crucial for managing the disease effectively. With a cost of 4400 AED, the test provides valuable insights into the condition, facilitating better treatment planning and support for patients. DNA Labs UAE remains committed to advancing genetic testing and support for individuals and families facing genetic disorders.
