Short Description

NGS genetic DNA test detecets for variant and mutation detection in PDCD10 gene for Cerebral cavernous malformations type 3

PreTest Information

Clinical History of Patient who is going for PDCD10 Gene Cerebral cavernous malformations type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PDCD10 Gene Cerebral cavernous malformations type 3 NGS Genetic DNA Test gene PDCD10

Detail Description

PDCD10 Gene and Cerebral Cavernous Malformations Type 3: Understanding Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

When it comes to cerebral cavernous malformations, or CCM, type 3 is one of the most severe forms of the disease. It is caused by a mutation in the PDCD10 gene, which is responsible for regulating the growth and development of blood vessels in the brain. This mutation can lead to the formation of abnormal blood vessels in the brain, which can cause a range of symptoms and complications.

What are the Symptoms of Cerebral Cavernous Malformations Type 3?

The symptoms of CCM type 3 can vary widely from person to person, but they often include:

• Seizures
• Headaches
• Difficulty speaking or understanding language
• Weakness or numbness on one side of the body
• Vision problems
• Problems with balance or coordination

If you experience any of these symptoms, it is important to seek medical attention right away. CCM type 3 can be a life-threatening condition if left untreated.

How is Cerebral Cavernous Malformations Type 3 Diagnosed?

Diagnosing CCM type 3 can be challenging, as the symptoms can be similar to those of other neurological conditions. Your doctor will likely start by taking a detailed medical history and performing a physical exam. They may also order one or more of the following tests:

• Magnetic resonance imaging (MRI)
• Computed tomography (CT) scan
• Electroencephalogram (EEG)
• Genetic testing

If genetic testing is performed, it will likely involve a Next-Generation Sequencing (NGS) DNA test. This test is designed to detect mutations in the PDCD10 gene that are associated with CCM type 3. The cost of an NGS genetic DNA test for CCM type 3 in India is typically around INR 20,000.

What are the Treatment Options for Cerebral Cavernous Malformations Type 3?

Currently, there is no cure for CCM type 3. Treatment is focused on managing symptoms and preventing complications. Depending on the severity of your symptoms, your doctor may recommend one or more of the following:

• Anti-seizure medications
• Pain relievers
• Physical therapy
• Surgery to remove the abnormal blood vessels

Your treatment plan will be tailored to your specific needs and circumstances. It is important to work closely with your healthcare team to manage your symptoms and prevent complications.

Conclusion

Cerebral cavernous malformations type 3 is a serious condition that can cause a range of symptoms and complications. If you are experiencing symptoms of CCM type 3, it is important to seek medical attention right away. A genetic test using Next-Generation Sequencing (NGS) technology can help diagnose the condition, with a cost of around INR 20,000 in India. While there is no cure for CCM type 3, there are treatment options available to manage symptoms and prevent complications.

For more information on genetic testing and treatment options for CCM type 3, contact DNA Labs India today.