Short Description

NGS genetic DNA test detecets for variant and mutation detection in CCT5 gene for Neuropathy, hereditary sensory, with spastic paraplegia

PreTest Information

Clinical History of Patient who is going for CCT5 Gene Neuropathy, hereditary sensory, with spastic paraplegia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CCT5 Gene Neuropathy, hereditary sensory, with spastic paraplegia

Detail Description

CCT5 Gene Neuropathy: Hereditary Sensory with Spastic Paraplegia

CCT5 gene neuropathy is a rare genetic disorder that affects the nervous system. It is characterized by a combination of sensory loss and spastic paraplegia. Hereditary sensory neuropathy is a condition that affects the nerves responsible for transmitting sensory information from the body to the brain. Spastic paraplegia is a condition that affects the muscles in the legs, causing stiffness and difficulty in walking.

Symptoms of CCT5 Gene Neuropathy

The symptoms of CCT5 gene neuropathy can vary from person to person. Some common symptoms include:

• Sensory loss in the hands and feet
• Difficulty in walking
• Muscle stiffness in the legs
• Weakness in the legs
• Difficulty in balancing
• Loss of bladder and bowel control
• Difficulty in speaking

Diagnosis of CCT5 Gene Neuropathy

CCT5 gene neuropathy is a genetic disorder that can be diagnosed through genetic testing. The most common method of genetic testing is Next Generation Sequencing (NGS) Genetic DNA Test. This test is used to analyze the DNA sequence of the CCT5 gene and identify any changes or mutations that may be causing the disorder.

Cost of NGS Genetic DNA Test for CCT5 Gene Neuropathy

The cost of NGS Genetic DNA Test for CCT5 Gene Neuropathy in India is approximately INR 20,000. However, the cost may vary depending on the location and the laboratory where the test is conducted.

Treatment for CCT5 Gene Neuropathy

Currently, there is no cure for CCT5 gene neuropathy. Treatment is focused on managing the symptoms and improving the quality of life of the patient. Physical therapy, occupational therapy, and speech therapy may be recommended to improve mobility, balance, and speech. Medications may also be prescribed to manage muscle stiffness and spasticity.

Conclusion

CCT5 gene neuropathy is a rare genetic disorder that affects the nervous system. It is characterized by a combination of sensory loss and spastic paraplegia. The disorder can be diagnosed through genetic testing, and the cost of NGS Genetic DNA Test in India is approximately INR 20,000. While there is no cure for CCT5 gene neuropathy, treatment can help manage the symptoms and improve the quality of life of the patient.

If you suspect that you or a loved one may have CCT5 gene neuropathy, it is important to consult a healthcare professional for an accurate diagnosis and appropriate treatment.

For more information on genetic testing for neurological disorders, contact DNA Labs India. Our team of experts can provide you with personalized genetic testing services to help you understand your genetic risk for various conditions.

Remember, early detection and intervention can make a significant difference in the management of genetic disorders.