Symptoms and Testing information for ARHGEF10 Gene Slowed Nerve Conduction Velocity Autosomal Dominant Genetic Test

Symptoms and Testing information for ARHGEF10 Gene Slowed Nerve Conduction Velocity Autosomal Dominant Genetic Test

The ARHGEF10 gene plays a crucial role in the development and function of the peripheral nervous system. Mutations in this gene have been linked to slowed nerve conduction velocity, a condition that affects the speed at which electrical signals travel along the nerves. This autosomal dominant trait means that only one copy of the altered gene is sufficient to cause the disorder. At DNA Labs UAE, we offer a comprehensive genetic test for identifying mutations in the ARHGEF10 gene, providing crucial information for affected individuals and their families. The cost of the test is 4400 AED.

Symptoms associated with ARHGEF10 gene mutation and slowed nerve conduction velocity can vary widely among individuals but typically include:

– Delayed motor milestones in children, such as walking or grasping
– Muscle weakness, often more pronounced in the lower limbs
– Decreased muscle tone and bulk
– Sensory disturbances, including numbness or tingling in the extremities
– Frequent falls or difficulty with coordination
– Chronic pain in affected limbs, sometimes described as burning or tingling

These symptoms result from the impaired transmission of electrical signals in the peripheral nerves, affecting both motor and sensory functions. It is important to note that the severity and specific symptoms can vary significantly from person to person, even among members of the same family.

The genetic test offered by DNA Labs UAE for the ARHGEF10 gene mutation is a crucial step in the diagnosis and management of slowed nerve conduction velocity. Early identification of the mutation can lead to more effective management strategies, including physical therapy, pain management, and, in some cases, surgical interventions. Furthermore, understanding the genetic basis of the condition can provide valuable information for family planning.

For more information on the ARHGEF10 gene slowed nerve conduction velocity autosomal dominant genetic test, please visit our website at [DNA Labs UAE](https://dnalabsuae.com/tests/arhgef10-gene-slowed-nerve-conduction-velocity-autosomal-dominant-genetic-test/).

Understanding ARHGEF10 Gene and Its Impact on Nerve Conduction Velocity

The ARHGEF10 gene plays a crucial role in the development and function of the peripheral nervous system. Mutations in this gene have been linked to slowed nerve conduction velocity, a condition that affects the speed at which electrical signals travel along the nerves. This autosomal dominant trait means that only one copy of the altered gene is sufficient to cause the disorder. At DNA Labs UAE, we offer a comprehensive genetic test for identifying mutations in the ARHGEF10 gene, providing crucial information for affected individuals and their families. The cost of the test is 4400 AED.

Symptoms of ARHGEF10 Gene Mutation

Symptoms associated with ARHGEF10 gene mutation and slowed nerve conduction velocity can vary widely among individuals but typically include:

  • Delayed motor milestones in children, such as walking or grasping
  • Muscle weakness, often more pronounced in the lower limbs
  • Decreased muscle tone and bulk
  • Sensory disturbances, including numbness or tingling in the extremities
  • Frequent falls or difficulty with coordination
  • Chronic pain in affected limbs, sometimes described as burning or tingling

These symptoms result from the impaired transmission of electrical signals in the peripheral nerves, affecting both motor and sensory functions. It is important to note that the severity and specific symptoms can vary significantly from person to person, even among members of the same family.

The Importance of Genetic Testing for ARHGEF10 Gene Mutation

The genetic test offered by DNA Labs UAE for the ARHGEF10 gene mutation is a crucial step in the diagnosis and management of slowed nerve conduction velocity. Early identification of the mutation can lead to more effective management strategies, including physical therapy, pain management, and, in some cases, surgical interventions. Furthermore, understanding the genetic basis of the condition can provide valuable information for family planning.

For more information on the ARHGEF10 gene slowed nerve conduction velocity autosomal dominant genetic test, please visit our website at DNA Labs UAE.

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