PreTest Information

Detail Description

CLN6 Additional Family Members Cost INR:14000 Symptoms Diagnosis

CLN6 is a rare genetic disorder that affects the nervous system. It is caused by a mutation in the CLN6 gene, which leads to the accumulation of toxic substances in the brain. The symptoms of CLN6 usually start to appear in early childhood and progress over time.

Symptoms of CLN6

The symptoms of CLN6 can vary from person to person, but some common signs and symptoms include:

• Vision loss
• Seizures
• Muscle stiffness
• Speech difficulties
• Behavioral changes
• Intellectual disability

If you suspect that your child may have CLN6, it is important to seek medical attention as soon as possible. Early diagnosis and treatment can help to manage the symptoms and improve the quality of life for the affected individual.

Diagnosis of CLN6

Diagnosing CLN6 can be challenging, as the symptoms can be similar to other neurological disorders. However, there are a few tests that can help to confirm a diagnosis, including:

• Genetic testing
• Brain imaging
• Electroencephalogram (EEG)

Genetic testing is the most reliable way to diagnose CLN6. It involves analyzing a blood or saliva sample to look for mutations in the CLN6 gene.

Additional Family Members Cost INR:14000

If a family member has already been diagnosed with CLN6, it is recommended that other family members undergo genetic testing as well. This can help to identify individuals who may be carriers of the gene mutation and are at risk of passing it on to their children.

The cost of genetic testing for additional family members is typically around INR 14000. This may vary depending on the testing facility and the specific tests that are ordered.

Conclusion

CLN6 is a rare genetic disorder that can be challenging to diagnose. However, early diagnosis and treatment can help to manage the symptoms and improve the quality of life for affected individuals. If you suspect that your child may have CLN6, it is important to seek medical attention as soon as possible. If a family member has already been diagnosed with CLN6, genetic testing for additional family members can help to identify carriers of the gene mutation and reduce the risk of passing it on to future generations.

At DNA Labs India, we offer genetic testing services for a variety of conditions, including CLN6. Our testing is reliable, accurate, and affordable. Contact us today to learn more about our services and how we can help you and your family.