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CAPN1 Gene Muscular-Skeletal Disorder CAPN1 Related Genetic Test Cost

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

-21%

The CAPN1 gene plays a crucial role in the development and maintenance of the musculoskeletal system. Mutations in the CAPN1 gene can lead to a variety of muscular and skeletal disorders, which can significantly impact an individual’s quality of life. These disorders are typically characterized by muscle weakness, atrophy, and sometimes skeletal abnormalities. Early detection and diagnosis through genetic testing are essential for managing symptoms and improving outcomes.

DNA Labs UAE offers a specialized genetic test aimed at identifying mutations in the CAPN1 gene. This test is a vital tool for individuals experiencing symptoms of muscular-skeletal disorders or those with a family history of such conditions. By analyzing the genetic makeup of an individual, the test can confirm the presence of CAPN1 gene mutations, providing crucial information for diagnosis and treatment planning.

The cost of the CAPN1 related genetic test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect any abnormalities associated with the CAPN1 gene. Results from this test can guide healthcare providers in developing personalized management plans, including physical therapy, medication, or other interventions aimed at improving patient outcomes. Early diagnosis through this genetic test can be instrumental in enhancing the quality of life for individuals affected by CAPN1 gene-related muscular-skeletal disorders.

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CAPN1 Gene Muscular-skeletal Disorder Genetic Test

At DNA Labs UAE, we offer the CAPN1 Gene Muscular-skeletal Disorder Genetic Test for individuals who may be at risk of developing this disorder. This test helps diagnose the disorder and guide treatment decisions.

Test Details

The CAPN1 gene is responsible for encoding the calpain-1 protein, which plays a crucial role in muscle development and function. Mutations in the CAPN1 gene can lead to a muscular-skeletal disorder known as CAPN1-related disorder.

Our Next-Generation Sequencing (NGS) genetic test uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of CAPN1-related disorder, this test can identify mutations or variations in the CAPN1 gene associated with the disorder.

Components and Price

  • Test Name: CAPN1 Gene Muscular-skeletal Disorder CAPN1 related Genetic Test
  • 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

Test Process

The NGS genetic test for CAPN1-related disorder involves collecting a sample of DNA, usually through a blood or saliva sample, from the individual undergoing testing. The DNA is then sequenced using NGS technology to identify any variations or mutations in the CAPN1 gene.

Pre Test Information

Before undergoing the CAPN1 Gene Muscular-skeletal Disorder 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 by CAPN1 Gene Muscular-skeletal Disorder.

Who Should Take the Test?

Genetic testing for CAPN1-related disorder is typically recommended for individuals with symptoms suggestive of the disorder or a family history of the condition. The test is usually ordered by a healthcare provider specializing in genetics or genetic counseling.

Benefits of Genetic Testing

Genetic testing can provide valuable information about an individual’s risk of developing a particular disorder, help with diagnosis, and guide treatment decisions. However, it is important to discuss the benefits, limitations, and potential implications of genetic testing with a healthcare provider before undergoing any testing.

Test Name CAPN1 Gene Muscular-skeletal disorder CAPN1 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 CAPN1 Gene Muscular-skeletal disorder, CAPN1 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CAPN1 Gene Muscular-skeletal disorder, CAPN1 related
Test Details

The CAPN1 gene is responsible for encoding the calpain-1 protein, which plays a crucial role in muscle development and function. Mutations in the CAPN1 gene can lead to a muscular-skeletal disorder known as CAPN1-related disorder.

A NGS (Next-Generation Sequencing) genetic test is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of CAPN1-related disorder, a NGS genetic test can be used to identify mutations or variations in the CAPN1 gene that may be associated with the disorder.

The NGS genetic test for CAPN1-related disorder involves collecting a sample of DNA, usually through a blood or saliva sample, from the individual undergoing testing. The DNA is then sequenced using NGS technology to identify any variations or mutations in the CAPN1 gene. The results of the test can help diagnose the disorder and guide treatment decisions.

It is important to note that genetic testing for CAPN1-related disorder is typically performed in individuals with symptoms suggestive of the disorder or a family history of the condition. The test is usually ordered by a healthcare provider who specializes in genetics or genetic counseling.

Genetic testing can provide valuable information about an individual’s risk of developing a particular disorder, help with diagnosis, and guide treatment decisions. However, it is important to discuss the benefits, limitations, and potential implications of genetic testing with a healthcare provider before undergoing any testing.

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