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MYH7 Gene Myosin Storage Myopathy Genetic Test Cost

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

-21%

The MYH7 gene myosin storage myopathy genetic test is a specialized diagnostic procedure aimed at detecting mutations in the MYH7 gene, which is known to cause myosin storage myopathy (MSM). This condition is a rare genetic disorder affecting skeletal muscles, leading to muscle weakness and other symptoms. The test involves analyzing the patient’s DNA to identify any genetic alterations in the MYH7 gene that are indicative of the disease. Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, this test provides crucial information for the diagnosis, management, and understanding of myosin storage myopathy. The cost of the test is set at 4400 AED, reflecting the intricate processes and sophisticated technology employed in identifying the genetic mutations associated with this condition.

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MYH7 Gene Myosin Storage Myopathy Genetic Test

Welcome to DNA Labs UAE, where we offer the MYH7 Gene Myosin Storage Myopathy Genetic Test. This test is designed to diagnose and understand the underlying cause of myosin storage myopathy (MSM), a rare genetic disorder characterized by the accumulation of abnormal myosin proteins within muscle cells.

Test Details

The MYH7 gene is responsible for encoding the protein called myosin heavy chain 7, which plays a crucial role in muscle contraction. Mutations in this gene can lead to MSM. Symptoms of MSM include muscle weakness, fatigue, and difficulty with movement. The severity and specific symptoms can vary between affected individuals.

Components and Price

The MYH7 Gene Myosin Storage Myopathy Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card. The report will be delivered within 3 to 4 weeks.

Method and Test Type

The MYH7 Gene Myosin Storage Myopathy Genetic Test utilizes Next-Generation Sequencing (NGS) technology. NGS allows for the rapid and cost-effective sequencing of a large number of genes simultaneously. This test falls under the category of neurological disorders and is conducted by our team of expert neurologists in our Genetics department.

Pre Test Information

Before undergoing the MYH7 Gene Myosin Storage Myopathy Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by MSM. This information helps in understanding the inheritance pattern and assessing the risk of passing on the condition.

Benefits of the Test

NGS testing allows for the identification of specific genetic mutations in the MYH7 gene, providing a definitive diagnosis of MSM. This information is crucial for understanding the underlying cause of the condition, predicting disease progression, and guiding treatment decisions. It also plays a vital role in genetic counseling and family planning purposes.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to schedule your MYH7 Gene Myosin Storage Myopathy Genetic Test and gain valuable insights into your health.

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

The MYH7 gene is responsible for encoding the protein called myosin heavy chain 7, which is involved in muscle contraction. Mutations in this gene can lead to a condition known as myosin storage myopathy (MSM).

MSM is a rare genetic disorder characterized by the accumulation of abnormal myosin proteins within muscle cells. This buildup interferes with muscle function and can result in muscle weakness, fatigue, and difficulty with movement. The severity and specific symptoms of MSM can vary widely between affected individuals.

Next-generation sequencing (NGS) is a type of genetic test that allows for the rapid and cost-effective sequencing of a large number of genes simultaneously. It is commonly used to identify genetic mutations associated with various diseases, including MSM. NGS can analyze the MYH7 gene for any mutations or variants that may be causing the condition.

By identifying specific genetic mutations in the MYH7 gene, NGS testing can provide a definitive diagnosis of MSM. This information can be crucial for understanding the underlying cause of the condition, predicting disease progression, and guiding treatment decisions. It can also be helpful for genetic counseling and family planning purposes.

SKU: TEST-1812 Category:

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