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MYH7 Gene Scapuloperoneal Myopathy MYH7 Related Genetic Test Cost

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

-21%

The MYH7 gene plays a critical role in the body’s muscle function, particularly in the heart and skeletal muscles. Mutations in the MYH7 gene can lead to various myopathies, including Scapuloperoneal Myopathy, a rare genetic disorder characterized by progressive weakness and atrophy of the muscles in the shoulders (scapula) and legs (peroneal muscles). This condition can significantly impact an individual’s quality of life, making early and accurate diagnosis crucial for managing symptoms and planning treatment strategies.

To diagnose this condition, DNA Labs UAE offers a specialized genetic test that focuses on identifying mutations in the MYH7 gene related to Scapuloperoneal Myopathy. This test is a valuable tool for clinicians and genetic counselors in diagnosing patients with symptoms suggestive of MYH7-related conditions, allowing for a more targeted approach to treatment and management.

The cost of the MYH7-related genetic test at DNA Labs UAE is 4400 AED. The testing process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the lab for specific genetic mutations associated with the MYH7 gene. Results from this test can provide crucial information for affected individuals and their families, including the confirmation of a diagnosis, insights into the progression of the disease, and implications for other family members who may be at risk.

Given the specialized nature of this test and its importance in the diagnosis and management of Scapuloperoneal Myopathy, the investment in testing can be a critical step towards achieving a better understanding of the condition and improving patient care.

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MYH7 Gene Scapuloperoneal myopathy MYH7 related Genetic Test

Test Name: MYH7 Gene Scapuloperoneal myopathy MYH7 related 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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for MYH7 Gene Scapuloperoneal myopathy, MYH7 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYH7 Gene Scapuloperoneal myopathy, MYH7 related.

Test Details

The MYH7 gene is responsible for providing instructions for making a protein called beta-myosin heavy chain, which is a crucial component of muscle cells. Mutations in the MYH7 gene can lead to various muscle disorders, including scapuloperoneal myopathy.

Scapuloperoneal myopathy is a rare genetic disorder that primarily affects the muscles of the shoulder blades (scapulae) and lower legs (peroneal muscles). It is characterized by muscle weakness and wasting in these areas, leading to difficulties with walking, shoulder movement, and other muscle-related symptoms.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes, including the MYH7 gene. It is a more advanced and comprehensive method compared to traditional genetic testing techniques.

An MYH7-related NGS genetic test involves sequencing the MYH7 gene to identify any mutations or variations that may be present. This test can help in confirming a diagnosis of scapuloperoneal myopathy and identifying the specific mutation within the MYH7 gene that is causing the condition.

Genetic testing can be useful for individuals who have symptoms consistent with scapuloperoneal myopathy and want to confirm the diagnosis. It can also be valuable for family members of affected individuals who may be at risk of inheriting the condition.

It is important to note that genetic testing should be done under the guidance of a healthcare professional, such as a genetic counselor or medical geneticist, who can help interpret the results and provide appropriate counseling and management options based on the findings.

Test Name MYH7 Gene Scapuloperoneal myopathy MYH7 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 MYH7 Gene Scapuloperoneal myopathy, MYH7 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MYH7 Gene Scapuloperoneal myopathy, MYH7 related
Test Details

The MYH7 gene is responsible for providing instructions for making a protein called beta-myosin heavy chain, which is a crucial component of muscle cells. Mutations in the MYH7 gene can lead to various muscle disorders, including scapuloperoneal myopathy.

Scapuloperoneal myopathy is a rare genetic disorder that primarily affects the muscles of the shoulder blades (scapulae) and lower legs (peroneal muscles). It is characterized by muscle weakness and wasting in these areas, leading to difficulties with walking, shoulder movement, and other muscle-related symptoms.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes, including the MYH7 gene. It is a more advanced and comprehensive method compared to traditional genetic testing techniques.

An MYH7-related NGS genetic test involves sequencing the MYH7 gene to identify any mutations or variations that may be present. This test can help in confirming a diagnosis of scapuloperoneal myopathy and identifying the specific mutation within the MYH7 gene that is causing the condition.

Genetic testing can be useful for individuals who have symptoms consistent with scapuloperoneal myopathy and want to confirm the diagnosis. It can also be valuable for family members of affected individuals who may be at risk of inheriting the condition.

It is important to note that genetic testing should be done under the guidance of a healthcare professional, such as a genetic counselor or medical geneticist, who can help interpret the results and provide appropriate counseling and management options based on the findings.

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