Why to get tested at DNA Labs India for CSRP3 Gene Cardiomyopathy, familial hypertrophic type 12 NGS Genetic DNA Test ?
Book Now
-
3500 Sample collection centers, Free Home Sample
collection for CSRP3 Gene Cardiomyopathy, familial hypertrophic type 12 NGS Genetic DNA Test in your city
-
Ranked India No1 DNA Test Lab for
CSRP3 Gene Cardiomyopathy, familial hypertrophic type 12 NGS Genetic DNA Test
-
Most Trusted Lab by doctors for CSRP3 Gene Cardiomyopathy, familial hypertrophic type 12 NGS Genetic DNA Test. Call 07941057551 to talk with Doctor to
get second opinion for free of cost
-
100% All Conversation are private and confidential Call 07941057551 to talk with doctor 100%
Accurate Test Results for CSRP3 Gene Cardiomyopathy, familial hypertrophic type 12 NGS Genetic DNA Test
CSRP3 Gene Cardiomyopathy, familial hypertrophic type 12 NGS Genetic DNA Test Cost 20000 Rs
CSRP3 Gene Cardiomyopathy, familial hypertrophic type 12 NGS Genetic DNA Test Details
CSRP3 Gene Cardiomyopathy: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost
Cardiomyopathy is a disease of the heart muscle that affects its ability to pump blood effectively. Familial hypertrophic cardiomyopathy (FHC) is a form of cardiomyopathy that is inherited and affects both children and adults. It is caused by mutations in genes that encode proteins involved in the contraction of heart muscle cells.
One of these genes is the CSRP3 gene, which encodes a protein called cysteine and glycine-rich protein 3. Mutations in the CSRP3 gene have been linked to familial hypertrophic cardiomyopathy type 12.
Symptoms of CSRP3 Gene Cardiomyopathy
The symptoms of CSRP3 gene cardiomyopathy can vary widely, even among members of the same family who carry the same mutation. Some people may have no symptoms at all, while others may experience:
- Chest pain or discomfort
- Shortness of breath
- Fainting or dizziness
- Abnormal heart rhythms
- Swelling in the legs, ankles, or feet
These symptoms can be present at any age, but they often first appear during adolescence or early adulthood.
Diagnosis of CSRP3 Gene Cardiomyopathy
Diagnosing CSRP3 gene cardiomyopathy typically involves a combination of medical history, physical examination, and diagnostic tests. A doctor may ask about symptoms, family history, and any previous heart problems. They will also listen to the heart with a stethoscope to check for abnormal heart sounds and rhythms.
Diagnostic tests that may be used to diagnose CSRP3 gene cardiomyopathy include:
- Electrocardiogram (ECG) to measure the electrical activity of the heart
- Echocardiogram to create images of the heart
- Cardiac MRI to create detailed images of the heart and blood vessels
- Genetic testing to look for mutations in the CSRP3 gene
NGS Genetic DNA Test Cost
NGS (Next-Generation Sequencing) genetic DNA testing is a powerful tool that can help diagnose CSRP3 gene cardiomyopathy. It is a type of genetic test that can analyze large amounts of DNA at once, allowing for the detection of mutations in multiple genes. The cost of an NGS genetic DNA test for CSRP3 gene cardiomyopathy in India is around INR 20,000.
NGS genetic DNA testing can be done using a blood sample or a saliva sample. The sample is sent to a laboratory for analysis, and the results are usually available within a few weeks. If a mutation is found in the CSRP3 gene, the person may be diagnosed with CSRP3 gene cardiomyopathy and may require further testing and treatment.
Conclusion
CSRP3 gene cardiomyopathy is a rare form of familial hypertrophic cardiomyopathy that is caused by mutations in the CSRP3 gene. Symptoms can vary widely, and diagnosis typically involves a combination of medical history, physical examination, and diagnostic tests. NGS genetic DNA testing can help diagnose CSRP3 gene cardiomyopathy, with a cost of around INR 20,000 in India. If you suspect that you or a family member may have CSRP3 gene cardiomyopathy, talk to your doctor about diagnostic testing and treatment options.
