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MT-TC Gene MELAS syndrome Genetic Test Cost

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

-21%

The MT-TC Gene MELAS Syndrome Genetic Test is a specialized diagnostic assessment available at DNA Labs UAE, designed to detect mutations in the mitochondrial gene MT-TC, which are associated with Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes (MELAS) syndrome. MELAS is a rare genetic disorder that affects various systems of the body, particularly the nervous system and muscles, leading to a wide range of symptoms including muscle weakness, headaches, loss of appetite, and more.

This test is crucial for individuals who exhibit symptoms of MELAS syndrome or have a family history of mitochondrial disorders, as it helps in confirming the diagnosis, thereby facilitating appropriate treatment and management strategies. Conducted in a state-of-the-art facility, the test requires a sample of the patient’s blood or other tissues, which is then analyzed for specific genetic mutations.

The cost of the MT-TC Gene MELAS Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This investment is vital for those at risk, as early detection and understanding of the specific genetic mutation present can significantly impact the management approach, potentially improving quality of life and outcomes for affected individuals.

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MT-TC Gene MELAS syndrome Genetic Test

At DNA Labs UAE, we offer the MT-TC Gene MELAS syndrome Genetic Test for individuals who are experiencing symptoms consistent with MELAS syndrome or have a family history of the condition. This genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the MT-TC gene for mutations associated with MELAS syndrome.

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

Before undergoing the MT-TC Gene MELAS syndrome NGS Genetic DNA 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-TC Gene MELAS syndrome NGS Genetic DNA Test gene MT-TC.

Test Details

MELAS syndrome is a rare mitochondrial disorder that affects various systems in the body, including the brain, muscles, and blood vessels. The MT-TC gene encodes transfer RNA (tRNA) molecules responsible for protein synthesis within mitochondria. Mutations in this gene can lead to impaired mitochondrial function, resulting in the symptoms of MELAS syndrome.

The MT-TC Gene MELAS syndrome NGS Genetic Test utilizes NGS technology to analyze the MT-TC gene for both common and rare mutations associated with MELAS syndrome. This comprehensive assessment of genetic variations aids in the diagnosis and management of the condition.

Healthcare professionals can use the results of this genetic test to determine the underlying cause of symptoms and make informed treatment decisions. Furthermore, the test provides valuable information for family members who may be at risk of inheriting the mutation.

It is important to note that genetic testing should be interpreted by a qualified healthcare professional specializing in genetics or mitochondrial disorders.

Test Name MT-TC Gene MELAS syndrome 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-TC Gene MELAS syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TC Gene MELAS syndrome NGS Genetic DNA Test gene MT-TC
Test Details

MT-TC Gene MELAS syndrome NGS Genetic Test is a genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the MT-TC gene for mutations associated with MELAS syndrome. MELAS syndrome is a rare mitochondrial disorder that affects multiple systems in the body, including the brain, muscles, and blood vessels.

The MT-TC gene is responsible for encoding transfer RNA (tRNA) molecules that are involved in protein synthesis within mitochondria. Mutations in this gene can lead to impaired mitochondrial function, resulting in the symptoms of MELAS syndrome.

NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variations associated with MELAS syndrome. This test can identify both common and rare mutations in the MT-TC gene, aiding in the diagnosis and management of MELAS syndrome.

The results of the MT-TC Gene MELAS syndrome NGS Genetic Test can help healthcare professionals determine the underlying cause of symptoms and guide treatment decisions. Additionally, genetic testing can provide valuable information for family members who may be at risk of inheriting the mutation.

It is important to note that this test is typically performed on individuals who have symptoms consistent with MELAS syndrome or a family history of the condition. Genetic testing should be interpreted by a qualified healthcare professional who specializes in genetics or mitochondrial disorders.

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