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NEB Gene Nemaline Myopathy Type 2 Autosomal Recessive Genetic Test Cost

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

-21%

The NEB Gene Nemaline Myopathy Type 2 Autosomal Recessive Genetic Test is a specialized diagnostic examination designed to detect mutations in the NEB gene, which are responsible for causing Nemaline Myopathy Type 2 (NEM2). Nemaline Myopathy is a genetic muscle disorder characterized by muscle weakness, hypotonia, and the presence of rod-like structures in muscle cells, affecting individuals from infancy or early childhood. The condition is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

This genetic test is crucial for the accurate diagnosis of Nemaline Myopathy Type 2, enabling healthcare professionals to provide appropriate management and treatment options for affected individuals. It involves the collection of a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations in the NEB gene.

Performed at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates, the test ensures high accuracy and reliability. The cost of the NEB Gene Nemaline Myopathy Type 2 Autosomal Recessive Genetic Test is 4400 AED. Opting for this test at DNA Labs UAE offers individuals and families the advantage of accessing cutting-edge genetic testing technologies, expert interpretation of results, and comprehensive support throughout the testing process.

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NEB Gene Nemaline Myopathy Type 2 Autosomal Recessive Genetic Test

Welcome to DNA Labs UAE, a leading genetic laboratory offering the NEB Gene Nemaline Myopathy Type 2 Autosomal Recessive Genetic Test. In this blog, we will provide detailed information about the test, its components, cost, symptoms, diagnosis, and more.

Test Details

The NEB gene nemaline myopathy type 2 is a genetic disorder characterized by muscle weakness and wasting. It is caused by mutations in the NEB gene, which provides instructions for producing the protein nebulin. This condition follows an autosomal recessive inheritance pattern, meaning that an affected individual must inherit two copies of the mutated gene, one from each parent.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously for mutations. In the case of NEB gene nemaline myopathy type 2, NGS genetic testing can identify specific mutations in the NEB gene that are associated with this condition. This testing can help confirm a diagnosis and provide information about the genetic cause of the disorder.

Test Name

NEB Gene Nemaline Myopathy Type 2 Autosomal Recessive Genetic Test

Components

  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Price

AED 4400.0

Report Delivery

3 to 4 Weeks

Method

NGS Technology

Test Type

Neurological Disorders

Doctor

Neurologist

Test Department

Genetics

Pre Test Information

Before undergoing the NEB Gene Nemaline Myopathy Type 2 Autosomal Recessive Genetic 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 with NEB Gene Nemaline Myopathy Type 2 Autosomal Recessive.

Conclusion

If you suspect that you or someone you know may have nemaline myopathy type 2, it is recommended to consult with a healthcare professional or a genetic counselor who can provide further guidance and arrange for appropriate genetic testing.

Test Name NEB Gene Nemaline myopathy type 2 autosomal recessive 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 NEB Gene Nemaline myopathy type 2, autosomal recessive NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NEB Gene Nemaline myopathy type 2, autosomal recessive
Test Details

NEB gene nemaline myopathy type 2 is a genetic disorder characterized by muscle weakness and wasting. It is caused by mutations in the NEB gene, which provides instructions for producing the protein nebulin. This condition follows an autosomal recessive inheritance pattern, meaning that an affected individual must inherit two copies of the mutated gene, one from each parent.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously for mutations. In the case of NEB gene nemaline myopathy type 2, NGS genetic testing can identify specific mutations in the NEB gene that are associated with this condition. This testing can help confirm a diagnosis and provide information about the genetic cause of the disorder.

If you suspect that you or someone you know may have nemaline myopathy type 2, it is recommended to consult with a healthcare professional or a genetic counselor who can provide further guidance and arrange for appropriate genetic testing.

SKU: TEST-1820 Category:

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