FKTN Gene Cardiomyopathy dilated type 1X Genetic Test
At DNA Labs UAE, we offer the FKTN Gene Cardiomyopathy dilated type 1X Genetic Test for individuals who suspect or have been diagnosed with dilated cardiomyopathy. This genetic test focuses on detecting mutations or variations in the FKTN gene, which is associated with this specific type of cardiomyopathy.
Test Details
The FKTN gene cardiomyopathy, dilated type 1X is a type of genetic test that utilizes NGS (Next-Generation Sequencing) technology. NGS allows for the simultaneous analysis of multiple genes or regions of the genome, making it a highly efficient and accurate method for genetic testing.
In the context of cardiomyopathy, NGS can identify mutations or variations in the FKTN gene that may be responsible for the development of dilated cardiomyopathy. The FKTN gene encodes a protein called fukutin, which plays a crucial role in maintaining the structural integrity of muscle cells, including those in the heart. Mutations in the FKTN gene can lead to abnormal glycosylation of alpha-dystroglycan, resulting in the development of dilated cardiomyopathy.
Test Components
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Cardiovascular Pneumology Disorders
- Doctor: Cardiologist
- Test Department: Genetics
Symptoms and Diagnosis
Dilated cardiomyopathy is characterized by the enlargement and weakening of the heart muscle. Individuals with suspected or confirmed dilated cardiomyopathy may experience symptoms such as shortness of breath, fatigue, irregular heartbeat, and swelling in the legs and ankles. Diagnosis of dilated cardiomyopathy involves a thorough clinical evaluation, including medical history, physical examination, and various diagnostic tests such as echocardiogram, electrocardiogram, and cardiac MRI.
Pre Test Information
Prior to undergoing the FKTN Gene Cardiomyopathy dilated type 1X NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by FKTN Gene Cardiomyopathy dilated type 1X NGS Genetic DNA Test gene FKTN. This information helps healthcare professionals understand the genetic inheritance pattern and assess the risk of developing dilated cardiomyopathy.
Test Benefits
The FKTN Gene Cardiomyopathy dilated type 1X NGS genetic test can be beneficial in several ways. It can aid in the diagnosis of individuals with suspected or confirmed dilated cardiomyopathy, providing valuable information for healthcare professionals to confirm the diagnosis, understand the underlying genetic cause, and guide treatment and management strategies. Additionally, the test can be used for carrier testing in individuals with a family history of the condition, helping them make informed decisions regarding their healthcare.
Conclusion
Genetic testing, such as the FKTN Gene Cardiomyopathy dilated type 1X NGS genetic test, plays a crucial role in the diagnosis and management of dilated cardiomyopathy. By identifying mutations or variations in the FKTN gene, healthcare professionals can gain insights into the genetic factors contributing to the development of this condition. At DNA Labs UAE, we offer this advanced genetic test at a cost of 4400.0 AED. Contact us today to schedule an appointment or learn more about our services.
| Test Name | FKTN Gene Cardiomyopathy dilated type 1X Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Cardiovascular Pneumology Disorders |
| Doctor | Cardiologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for FKTN Gene Cardiomyopathy, dilated type 1X NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FKTN Gene Cardiomyopathy, dilated type 1X NGS Genetic DNA Test gene FKTN |
| Test Details |
FKTN gene cardiomyopathy, dilated type 1X is a type of genetic test that focuses on detecting mutations or variations in the FKTN gene. This gene is associated with a specific type of cardiomyopathy called dilated cardiomyopathy, which is characterized by the enlargement and weakening of the heart muscle. NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes or regions of the genome. In the context of genetic testing for cardiomyopathy, NGS can be used to identify mutations or variations in the FKTN gene, which may be responsible for the development of dilated cardiomyopathy. The FKTN gene encodes a protein called fukutin, which is involved in the glycosylation of alpha-dystroglycan, a protein that plays a crucial role in maintaining the structural integrity of muscle cells, including those in the heart. Mutations in the FKTN gene can lead to abnormal glycosylation of alpha-dystroglycan, resulting in the development of dilated cardiomyopathy. The FKTN gene cardiomyopathy, dilated type 1X NGS genetic test can help in the diagnosis of individuals with suspected or confirmed dilated cardiomyopathy. It can also be used for carrier testing in individuals with a family history of the condition. The test involves analyzing the DNA sample of the individual to identify any mutations or variations in the FKTN gene that may be contributing to the development of cardiomyopathy. The results of the genetic test can provide valuable information for healthcare professionals in terms of confirming the diagnosis, understanding the underlying genetic cause, and guiding treatment and management strategies for affected individuals and their families. Genetic counseling is often recommended before and after undergoing genetic testing to help individuals understand the implications of the test results and make informed decisions regarding their healthcare. |
