Short Description

NGS genetic DNA test detecets for variant and mutation detection in ARHGEF10 gene for Slowed nerve conduction velocity, autosomanal dominant

PreTest Information

Clinical History of Patient who is going for ARHGEF10 Gene Slowed nerve conduction velocity, autosomanal dominant NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ARHGEF10 Gene Slowed nerve conduction velocity, autosomanal dominant

Detail Description

ARHGEF10 Gene and Slowed Nerve Conduction Velocity: Understanding the Role of Autosomal Dominant NGS Genetic DNA Test

ARHGEF10 gene is a crucial gene that plays a vital role in the development of the nervous system. It is responsible for encoding a protein that is involved in the regulation of the actin cytoskeleton, which is essential for proper nerve conduction. Any mutation in this gene can lead to slowed nerve conduction velocity, which can cause a variety of symptoms and conditions.

Understanding Autosomal Dominant NGS Genetic DNA Test

Autosomal dominant NGS genetic DNA test is a sophisticated genetic test that can detect any mutation in the ARHGEF10 gene. It is a non-invasive test that uses advanced next-generation sequencing (NGS) technology to analyze the DNA sequence of the gene and identify any abnormalities. The test is highly accurate and can detect even the smallest genetic changes that can cause slowed nerve conduction velocity.

Symptoms of Slowed Nerve Conduction Velocity

Slowed nerve conduction velocity can cause a range of symptoms, depending on the severity of the condition. Some of the common symptoms include:

• Numbness or tingling sensation in the affected area
• Weakness or fatigue in the muscles
• Burning or shooting pain
• Difficulty in walking or moving the affected limb
• Loss of balance or coordination

Diagnosis of Slowed Nerve Conduction Velocity

Diagnosis of slowed nerve conduction velocity requires a thorough neurological examination and a series of tests. The doctor may recommend an electromyography (EMG) test, which measures the electrical activity of the muscles and the nerves. A nerve conduction study (NCS) may also be performed to evaluate the speed and strength of the nerve impulses. If the doctor suspects a genetic cause, an autosomal dominant NGS genetic DNA test may be recommended.

Cost of Autosomal Dominant NGS Genetic DNA Test in India

The cost of an autosomal dominant NGS genetic DNA test in India can vary depending on the laboratory and the location. However, on average, the cost of the test is around INR 20,000.

Conclusion

Slowed nerve conduction velocity can cause a range of symptoms and can be caused by mutations in the ARHGEF10 gene. An autosomal dominant NGS genetic DNA test is a non-invasive and accurate way to detect any genetic changes that can cause the condition. If you or a loved one is experiencing symptoms of slowed nerve conduction velocity, it is essential to seek medical attention and consider genetic testing to get an accurate diagnosis and appropriate treatment.

Contact DNA Labs India for an accurate autosomal dominant NGS genetic DNA test. Our team of experts uses advanced technology and provides fast and reliable results to help you get the answers you need.