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SGCD Gene Cardiomyopathy dilated type 1L Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

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The SGCD Gene Cardiomyopathy Dilated Type 1L Genetic Test is a specialized diagnostic tool used to identify mutations in the SGCD gene, which are associated with Dilated Cardiomyopathy Type 1L (DCM1L). This condition is a form of heart disease that affects the heart’s ability to pump blood efficiently, leading to heart enlargement and impaired systolic function. The SGCD gene plays a crucial role in encoding a part of the dystrophin-glycoprotein complex, which is essential for maintaining the integrity and function of muscle cells, including those in the heart.

The test is particularly valuable for individuals with a family history of DCM1L or symptoms suggestive of cardiomyopathy, such as shortness of breath, fatigue, or irregular heartbeats. Early detection through this genetic test can aid in the timely management and treatment of the condition, potentially improving the quality of life and prognosis for affected individuals.

Administered at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates, the test involves a simple blood draw or cheek swab from the patient. The sample is then analyzed for specific mutations in the SGCD gene that are linked to Dilated Cardiomyopathy Type 1L.

The cost of the SGCD Gene Cardiomyopathy Dilated Type 1L Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the comprehensive insight it provides into the genetic basis of cardiomyopathy can be invaluable for affected individuals and their families, offering a pathway to personalized medical care and interventions that can mitigate the impact of the disease.

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SGCD Gene Cardiomyopathy dilated type 1L Genetic Test

At DNA Labs UAE, we offer the SGCD Gene Cardiomyopathy dilated type 1L Genetic Test at a cost of AED 4400.0. This test is used to diagnose and identify mutations in the SGCD gene that are associated with 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

Pre Test Information

Prior to the SGCD Gene Cardiomyopathy dilated type 1L Genetic Test, it is important to provide the clinical history of the patient who is undergoing the test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by SGCD Gene Cardiomyopathy dilated type 1L NGS Genetic DNA Test gene SGCD.

Test Details

SGCD gene cardiomyopathy, dilated type 1L (also known as CMD1L) is a genetic disorder that affects the heart muscle, leading to the development of dilated cardiomyopathy. This condition is caused by mutations in the SGCD gene, which is responsible for producing a protein called delta-sarcoglycan.

Delta-sarcoglycan is part of a group of proteins that form a complex called the dystrophin-associated glycoprotein complex (DAGC). This complex plays a crucial role in maintaining the structural integrity of muscle cells, including those in the heart. However, mutations in the SGCD gene disrupt the normal function of the DAGC, resulting in the weakening and enlargement of the heart muscle.

NGS (Next-Generation Sequencing) genetic testing is utilized to analyze multiple genes simultaneously. In the case of SGCD gene cardiomyopathy, dilated type 1L, NGS genetic testing can identify mutations in the SGCD gene associated with the condition. This testing helps confirm a diagnosis, provide information about disease prognosis, and guide treatment decisions.

It is important to note that genetic testing for SGCD gene cardiomyopathy, dilated type 1L is typically recommended for individuals with a suspected or confirmed diagnosis of dilated cardiomyopathy, particularly if there is a family history of the condition. Genetic counseling is often advised both before and after testing to ensure individuals fully understand the implications of the test results and can make informed decisions about their healthcare.

Test Name SGCD Gene Cardiomyopathy dilated type 1L 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 SGCD Gene Cardiomyopathy, dilated type 1L NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SGCD Gene Cardiomyopathy, dilated type 1L NGS Genetic DNA Test gene SGCD
Test Details

SGCD gene cardiomyopathy, dilated type 1L (also known as CMD1L) is a genetic disorder that affects the heart muscle, leading to the development of dilated cardiomyopathy. It is caused by mutations in the SGCD gene, which provides instructions for making a protein called delta-sarcoglycan.

Delta-sarcoglycan is part of a group of proteins that form a complex called the dystrophin-associated glycoprotein complex (DAGC). This complex helps maintain the structural integrity of muscle cells, including those in the heart. Mutations in the SGCD gene disrupt the normal function of the DAGC, leading to the weakening and enlargement of the heart muscle.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of SGCD gene cardiomyopathy, dilated type 1L, NGS genetic testing can identify mutations in the SGCD gene that are associated with the condition. This testing can help confirm a diagnosis, provide information about disease prognosis, and guide treatment decisions.

It is important to note that genetic testing for SGCD gene cardiomyopathy, dilated type 1L is typically performed in individuals with a suspected or confirmed diagnosis of dilated cardiomyopathy, especially if there is a family history of the condition. Genetic counseling is often recommended before and after testing to help individuals understand the implications of the test results and make informed decisions about their healthcare.

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