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DNM2 Gene Centronuclear Myopathy Type 1 Genetic Test

4,400 د.إ

-21%

The DNM2 Gene Centronuclear Myopathy Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the DNM2 gene, which are responsible for Centronuclear Myopathy Type 1. This condition is a rare genetic disorder characterized by muscle weakness and abnormalities in the placement of nuclei in muscle cells. The test is crucial for early diagnosis, enabling timely intervention and management of the condition. Priced at 4400 AED, the test involves analyzing the patient’s DNA to identify specific genetic alterations in the DNM2 gene, providing insights into the risk and guiding treatment options for affected individuals and their families.

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DNM2 Gene Centronuclear Myopathy Type 1 Genetic Test

Centronuclear myopathy type 1 is a rare genetic disorder that affects muscle function. DNA Labs UAE offers a comprehensive genetic test for this condition.

Test Name: DNM2 Gene Centronuclear Myopathy Type 1 Genetic Test

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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the DNM2 Gene Centronuclear Myopathy Type 1 Genetic Test, it is important to provide the clinical history of the patient. A genetic counseling session may also be conducted to draw a pedigree chart of family members affected with DNM2 Gene Centronuclear Myopathy Type 1.

Test Details

The DNM2 gene is associated with centronuclear myopathy type 1. This genetic test uses NGS technology to analyze the patient’s DNA and identify any changes or mutations in the DNM2 gene. The results of this test can help diagnose centronuclear myopathy type 1 and guide treatment options. Additionally, it can identify carriers of the gene mutation and provide valuable information for family planning decisions.

Test Name DNM2 Gene Centronuclear myopathy type 1 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 DNM2 Gene Centronuclear myopathy type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DNM2 Gene Centronuclear myopathy type 1
Test Details

The DNM2 gene is associated with centronuclear myopathy type 1, a rare genetic disorder that affects muscle function. NGS genetic testing can identify mutations in the DNM2 gene that can cause this condition. This test involves analyzing the patient’s DNA to identify any changes or mutations in the DNM2 gene. The results of this test can help diagnose centronuclear myopathy type 1 and guide treatment options. It can also help identify carriers of the gene mutation and inform family planning decisions.