Short Description

NGS genetic DNA test detecets for variant and mutation detection in LRSAM1 gene for CMT2P

PreTest Information

Clinical History of Patient who is going for LRSAM1 Gene CMT2P NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with LRSAM1 Gene CMT2P

Detail Description

LRSAM1 Gene CMT2P NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis

Are you or your loved one experiencing muscle weakness, numbness, or tingling in your limbs? These symptoms could be indicative of Charcot-Marie-Tooth disease (CMT), a hereditary disorder that affects the nerves in the feet, legs, hands, and arms.

CMT is caused by a genetic mutation that affects the peripheral nerves, which are responsible for sending signals from the brain and spinal cord to the rest of the body. There are several different types of CMT, each with its own set of genetic mutations and symptoms.

One of the more rare forms of CMT is CMT2P, which is caused by a mutation in the LRSAM1 gene. If you suspect that you or a loved one may have CMT2P, it is essential to get a proper diagnosis so that you can receive appropriate treatment.

One way to diagnose CMT2P is through a genetic DNA test. This test can identify the specific genetic mutations associated with CMT2P, including mutations in the LRSAM1 gene.

What is an NGS Genetic DNA Test?

NGS (Next-Generation Sequencing) is a type of genetic DNA test that uses cutting-edge technology to examine an individual's DNA. This test can detect mutations in specific genes, including the LRSAM1 gene.

NGS is a highly accurate test that can provide a definitive diagnosis for CMT2P and other hereditary disorders.

How Much Does an NGS Genetic DNA Test Cost?

The cost of an NGS genetic DNA test can vary depending on the provider. At DNA Labs India, the cost for an NGS genetic DNA test for CMT2P is INR 20,000.

This cost may seem high, but it is important to remember that an accurate diagnosis can help you receive appropriate treatment and manage your symptoms. Additionally, many insurance companies may cover the cost of genetic testing for hereditary disorders like CMT2P.

What are the Symptoms of CMT2P?

The symptoms of CMT2P can vary from person to person and may include:

• Muscle weakness in the feet, legs, hands, or arms
• Numbness or tingling in the limbs
• Difficulty with balance and coordination
• Hammertoes or high arches in the feet
• Weakness in the muscles of the face and throat

If you are experiencing any of these symptoms, it is important to see a medical professional for a proper diagnosis.

How is CMT2P Diagnosed?

CMT2P is typically diagnosed through a combination of physical exams, medical history, and genetic testing. A medical professional will examine your muscles and nerves and may order tests like an electromyography (EMG) or nerve conduction study (NCS).

If CMT2P is suspected, a genetic DNA test can confirm the diagnosis and identify the specific genetic mutation causing the disorder.

Conclusion

CMT2P can be a challenging disorder to diagnose and manage, but an NGS genetic DNA test can provide a definitive diagnosis and help individuals receive appropriate treatment. If you suspect that you or a loved one may have CMT2P, it is essential to see a medical professional and consider genetic testing.

At DNA Labs India, we offer affordable and accurate genetic testing for a variety of hereditary disorders, including CMT2P. Contact us today to learn more about our services and how we can help you get the answers you need.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for LRSAM1 Gene CMT2P NGS Genetic DNA Test