Short Description

NGS genetic DNA test detecets for variant and mutation detection in KRIT1 gene for Cerebral cavernous malformations type 1

PreTest Information

Clinical History of Patient who is going for KRIT1 Gene Cerebral cavernous malformations type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KRIT1 Gene Cerebral cavernous malformations type 1 NGS Genetic DNA Test gene KRIT1

Detail Description

Understanding KRIT1 Gene and Cerebral Cavernous Malformations Type 1 NGS Genetic DNA Test

If you or your loved ones are experiencing symptoms like seizures, headaches, and weakness on one side of the body, it may be time to consider getting a genetic test to check for cerebral cavernous malformations type 1 (CCM1). This genetic disorder affects blood vessels in the brain and can lead to serious health complications.

What is KRIT1 Gene?

KRIT1 (Krev Interaction Trapped 1) is a gene that provides instructions for making a protein that helps to form and maintain blood vessels in the brain. Mutations in this gene can cause cerebral cavernous malformations type 1 (CCM1), a condition characterized by the development of abnormal blood vessels in the brain.

What are Cerebral Cavernous Malformations Type 1?

Cerebral cavernous malformations type 1 (CCM1) is a genetic disorder that affects blood vessels in the brain. The abnormal blood vessels are prone to leaking and can cause seizures, headaches, and weakness on one side of the body. In severe cases, CCM1 can lead to hemorrhagic stroke or permanent brain damage.

What is NGS Genetic DNA Test?

Next-generation sequencing (NGS) genetic DNA test is a sophisticated diagnostic tool that uses advanced sequencing technology to analyze multiple genes at once. This test can detect genetic mutations that may cause CCM1 and other inherited diseases.

What is the Cost of CCM1 NGS Genetic DNA Test in India?

The cost of CCM1 NGS genetic DNA test in India is approximately INR 20,000. However, the cost may vary depending on the testing facility and the specific genes being analyzed.

What are the Symptoms of CCM1?

The symptoms of CCM1 can vary from person to person and may include:

• Seizures
• Headaches
• Weakness on one side of the body
• Nausea and vomiting
• Difficulty speaking or understanding speech

How is CCM1 Diagnosed?

CCM1 can be diagnosed through genetic testing, imaging tests, or a combination of both. NGS genetic DNA test is a reliable method for detecting genetic mutations that may cause CCM1. Imaging tests like MRI or CT scan can help to visualize abnormal blood vessels in the brain.

Conclusion

CCM1 is a serious genetic disorder that affects blood vessels in the brain and can lead to seizures, headaches, and other neurological symptoms. NGS genetic DNA test is a reliable diagnostic tool that can detect genetic mutations that may cause CCM1. The cost of CCM1 NGS genetic DNA test in India is approximately INR 20,000. If you or your loved ones are experiencing symptoms of CCM1, it is important to seek medical attention and consider getting a genetic test to check for this condition.

For more information on genetic testing for CCM1, contact DNA Labs India today.