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MT-TE Gene Mitochondrial myopathy infantile transient MT-TE related Genetic Test Cost

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

-21%

The MT-TE gene plays a crucial role in the proper functioning of mitochondria, the powerhouses of the cell, by encoding for mitochondrial tRNA glutamic acid. Mutations in the MT-TE gene can lead to mitochondrial myopathy, a group of neuromuscular disorders characterized by muscle weakness and exercise intolerance. One specific condition associated with mutations in this gene is infantile transient mitochondrial myopathy, a rare disorder that presents early in life but often shows improvement with age.

To diagnose conditions related to the MT-TE gene, genetic testing is a critical tool. DNA Labs UAE offers a specialized genetic test designed to identify mutations in the MT-TE gene that are associated with mitochondrial myopathy, particularly the infantile transient type. This test is essential for confirming the diagnosis, understanding the disease’s progression, and informing treatment decisions.

The cost of the MT-TE gene mitochondrial myopathy genetic test at DNA Labs UAE is 4400 AED. Conducting this test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the lab for the presence of specific genetic mutations in the MT-TE gene. The results of this test can provide valuable information for affected individuals and their families, including the potential for genetic counseling and the exploration of targeted treatment options.

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MT-TE Gene Mitochondrial Myopathy Infantile Transient MT-TE Related Genetic Test

Welcome to DNA Labs UAE, where we offer the MT-TE Gene Mitochondrial Myopathy Infantile Transient MT-TE Related Genetic Test. This test is designed to diagnose and provide information about the genetic cause of MT-TE related mitochondrial myopathy, a type of mitochondrial myopathy that occurs in infants and resolves over time.

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: Cardiovascular Pneumology Disorders
  • Doctor: Cardiologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the MT-TE Gene Mitochondrial Myopathy Infantile Transient MT-TE Related 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 MT-TE Gene Mitochondrial Myopathy Infantile Transient MT-TE Related NGS Genetic DNA Test gene MT-TE.

Test Details

MT-TE gene mitochondrial myopathy is a type of mitochondrial myopathy caused by mutations in the MT-TE gene. Mitochondrial myopathies are genetic disorders that affect the energy-producing structures within cells called mitochondria. Infantile transient MT-TE related mitochondrial myopathy specifically refers to a form of the condition that occurs in infants and resolves over time. This form of mitochondrial myopathy is caused by mutations in the MT-TE gene.

NGS (Next-Generation Sequencing) genetic testing is a powerful tool used to identify genetic mutations. It allows for the simultaneous sequencing of multiple genes or even the entire genome. The NGS genetic test for MT-TE related mitochondrial myopathy involves analyzing the DNA sequence of the MT-TE gene to identify any mutations or variations. This test can confirm a diagnosis and provide information about the specific genetic cause of the condition.

Genetic testing is recommended for individuals with symptoms consistent with mitochondrial myopathy or a family history of the condition. It can provide a definitive diagnosis, guide treatment and management options, and offer important information for at-risk family members.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our MT-TE Gene Mitochondrial Myopathy Infantile Transient MT-TE Related Genetic Test can help diagnose and understand MT-TE related mitochondrial myopathy. Contact us today to learn more or schedule an appointment.

Test Name MT-TE Gene Mitochondrial myopathy infantile transient MT-TE 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 Cardiovascular Pneumology Disorders
Doctor Cardiologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MT-TE Gene Mitochondrial myopathy, infantile, transient, MT-TE related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TE Gene Mitochondrial myopathy, infantile, transient, MT-TE related NGS Genetic DNA Test gene MT-TE
Test Details

MT-TE gene mitochondrial myopathy is a type of mitochondrial myopathy that is caused by mutations in the MT-TE gene. Mitochondrial myopathies are a group of genetic disorders that affect the mitochondria, which are the energy-producing structures within cells.

Infantile transient MT-TE related mitochondrial myopathy refers to a specific form of the condition that occurs in infants and is transient, meaning it resolves over time. This form of mitochondrial myopathy is specifically caused by mutations in the MT-TE gene.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes or even the entire genome. It is a powerful tool for identifying genetic mutations and can be used to diagnose mitochondrial myopathies, including those caused by mutations in the MT-TE gene.

The NGS genetic test for MT-TE related mitochondrial myopathy involves analyzing the DNA sequence of the MT-TE gene to identify any mutations or variations that may be present. This can help confirm a diagnosis and provide information about the specific genetic cause of the condition.

Genetic testing can be helpful in providing a definitive diagnosis for individuals with suspected mitochondrial myopathy, as well as guiding treatment and management options. It can also provide important information for family members who may be at risk of inheriting the condition. However, it is important to note that genetic testing is typically only recommended for individuals who have symptoms consistent with mitochondrial myopathy or who have a family history of the condition.

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