Symptoms and Testing information for CHMP2B Gene Amyotrophic lateral sclerosis type 17 Genetic Test

Symptoms and Testing information for CHMP2B Gene Amyotrophic lateral sclerosis type 17 Genetic Test

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease, is a progressive neurodegenerative disorder that affects nerve cells in the brain and spinal cord. This condition leads to muscle weakness, disability, and eventually, death. ALS is characterized by its heterogeneity, with numerous genetic variations contributing to its onset and progression. Among these genetic factors, mutations in the CHMP2B gene have been identified as a rare cause, leading to a subtype of the disease known as ALS type 17. Recognizing the symptoms of this genetic variant is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for CHMP2B gene mutations, providing insights into one’s genetic predisposition to ALS type 17.

Symptoms of CHMP2B Gene Amyotrophic Lateral Sclerosis Type 17

The symptoms of ALS type 17, caused by mutations in the CHMP2B gene, share similarities with other forms of ALS but can exhibit unique characteristics. Initially, individuals may experience subtle changes in muscle strength, often starting in one area of the body and gradually spreading. Symptoms include:

  • Weakness in the limbs, often starting with the hands or legs
  • Muscle cramps and twitching
  • Difficulty with speech and swallowing
  • Impaired use of arms and legs
  • Increased muscle stiffness (spasticity)
  • Breathing difficulties as the disease progresses

As ALS type 17 advances, symptoms become more pronounced, leading to significant physical disabilities. It is important to note that cognitive functions may remain intact, distinguishing it from other forms of ALS where cognitive impairment can be prevalent.

CHMP2B Gene Amyotrophic Lateral Sclerosis Type 17 Genetic Test

DNA Labs UAE is at the forefront of genetic testing, offering a specialized test for the CHMP2B gene mutation associated with ALS type 17. This test is designed to detect the presence of mutations in the CHMP2B gene, providing valuable information for individuals with a family history of ALS or those experiencing symptoms suggestive of the disease. The process involves a simple blood draw or saliva sample, which is then analyzed in our state-of-the-art laboratory.

The cost of the CHMP2B gene amyotrophic lateral sclerosis type 17 genetic test is 4400 AED. This price includes the cost of the sample collection kit, laboratory analysis, and a comprehensive report detailing the findings. The report not only indicates the presence or absence of CHMP2B gene mutations but also provides guidance on the next steps, including potential treatment strategies and lifestyle adjustments.

Understanding one’s genetic risk can be a powerful tool in managing and potentially mitigating the impact of ALS. Early detection through genetic testing allows for prompt intervention, which can improve the quality of life and extend survival for those affected by the disease.

For more information about the CHMP2B gene amyotrophic lateral sclerosis type 17 genetic test and to schedule your testing, please visit our website at

At DNA Labs UAE, we are committed to providing accurate, confidential, and timely genetic testing services. Our team of experts is here to support you through the testing process and beyond, offering guidance and counseling to help you understand your results and their implications for your health and well-being.

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