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LMNA Gene Muscular Dystrophy Congenital LMNA Related Genetic Test

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

-21%

The LMNA gene muscular dystrophy, also known as congenital LMNA-related muscular dystrophy, is a rare genetic disorder characterized by muscle weakness and wasting. This condition is caused by mutations in the LMNA gene, which provides instructions for making a protein that is essential for the structural integrity and function of cells in the body. Individuals affected by this condition may experience symptoms ranging from mild to severe, including muscle weakness, cardiac issues, and skeletal abnormalities.

To diagnose this condition, a genetic test is available at DNA Labs UAE, which specifically looks for mutations in the LMNA gene associated with muscular dystrophy. The test is a crucial step in confirming the diagnosis, understanding the severity of the condition, and guiding treatment and management decisions.

The cost of the LMNA-related genetic test at DNA Labs UAE is 4400 AED. This test is performed using a sample of the patient’s blood or saliva, and it involves analyzing the DNA to identify any mutations in the LMNA gene. Results from this test can provide valuable information for affected individuals and their families regarding prognosis, potential interventions, and genetic counseling.

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LMNA Gene Muscular Dystrophy Congenital LMNA Related Genetic Test

At DNA Labs UAE, we offer the LMNA Gene Muscular Dystrophy Congenital LMNA Related Genetic Test. This test is designed to detect mutations in the LMNA gene, which are associated with a specific type of muscular dystrophy known as congenital muscular dystrophy.

Test Components

The test includes the following 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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the LMNA Gene Muscular Dystrophy Congenital LMNA Related Genetic Test, it is important to provide the following information:

  • Clinical History of Patient who is going for LMNA Gene Muscular Dystrophy, congenital, LMNA related NGS Genetic DNA Test
  • A Genetic Counselling session to draw a pedigree chart of family members affected with LMNA Gene Muscular Dystrophy, congenital, LMNA related

Test Details

The Muscular Dystrophy Congenital LMNA-related NGS genetic test is a powerful tool used to identify mutations in the LMNA gene. This gene is associated with congenital muscular dystrophy, a genetic disorder characterized by muscle weakness and wasting present from birth or early infancy.

The NGS (Next-Generation Sequencing) technology employed in this test enables the simultaneous analysis of multiple genes, including the LMNA gene. By doing so, it can accurately detect disease-causing mutations. This test is crucial for confirming a diagnosis of LMNA-related congenital muscular dystrophy and can also be used for carrier testing and prenatal diagnosis in families with a known history of this condition.

Genetic testing for LMNA-related congenital muscular dystrophy provides valuable information for individuals and their families. It helps determine the risk of passing on the condition to future generations, explore potential treatment options, and receive genetic counseling. This test is typically recommended for individuals with symptoms indicative of this condition or those with a family history of LMNA-related muscular dystrophy.

Test Name LMNA Gene Muscular dystrophy congenital LMNA related Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for LMNA Gene Muscular dystrophy, congenital, LMNA related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with LMNA Gene Muscular dystrophy, congenital, LMNA related
Test Details

Muscular dystrophy, congenital, LMNA-related NGS genetic test is a genetic test that is used to detect mutations in the LMNA gene. LMNA gene mutations are associated with a specific type of muscular dystrophy known as congenital muscular dystrophy. This genetic disorder is characterized by muscle weakness and wasting that is present from birth or early infancy.

The NGS (Next-Generation Sequencing) technology used in this test allows for the simultaneous analysis of multiple genes, including the LMNA gene, to identify any disease-causing mutations. This test can help in confirming a diagnosis of LMNA-related congenital muscular dystrophy and can also be used for carrier testing and prenatal diagnosis in families with a known history of this condition.

Genetic testing for LMNA-related congenital muscular dystrophy can provide important information for individuals and their families, including the risk of passing on the condition to future generations, potential treatment options, and genetic counseling. It is typically recommended for individuals with symptoms suggestive of this condition or those with a family history of LMNA-related muscular dystrophy.

SKU: TEST-1750 Category:

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