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MT-TR Gene Encephalomyopathy mitochondrial MT-TR related Genetic Test

4,400 د.إ

-21%

The MT-TR gene encephalomyopathy mitochondrial MT-TR related genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the MT-TR gene that are associated with mitochondrial encephalomyopathy. This condition is a complex mitochondrial disorder characterized by neurological and muscular impairments, resulting from dysfunctional energy production in the mitochondria. The MT-TR gene plays a crucial role in the mitochondrial function, and mutations in this gene can lead to a range of symptoms, including muscle weakness, neurological deficits, and systemic energy metabolism issues.

The test involves analyzing the patient’s DNA to detect mutations in the MT-TR gene, providing valuable information for diagnosis, prognosis, and treatment planning. It is a critical tool for clinicians in the management of patients with suspected mitochondrial disorders, offering insights that can guide personalized treatment approaches.

DNA Labs UAE offers this comprehensive genetic test for a cost of 4400 AED. The test is conducted in their state-of-the-art laboratory facilities, where they utilize advanced genetic sequencing technologies to ensure accurate and reliable results. Patients considering this test are usually referred by their healthcare provider based on clinical symptoms and family history suggestive of mitochondrial encephalomyopathy. The results from this test can significantly impact patient care, offering a clearer understanding of the disease mechanism and potential therapeutic interventions.

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MT-TR Gene Encephalomyopathy mitochondrial MT-TR related Genetic Test

Test Name: MT-TR Gene Encephalomyopathy mitochondrial MT-TR related Genetic Test

Components: NGS Technology

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 MT-TR Gene Encephalomyopathy, mitochondrial, MT-TR related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TR Gene Encephalomyopathy, mitochondrial, MT-TR related.

Test Details

Encephalomyopathy, mitochondrial, MT-TR related NGS genetic test is a type of genetic testing that analyzes the MT-TR gene for mutations that may cause mitochondrial encephalomyopathy. Mitochondrial encephalomyopathy is a rare genetic disorder that affects the brain and muscles. The MT-TR gene provides instructions for making a protein called mitochondrial transfer RNA, which is involved in the production of energy within cells. Mutations in the MT-TR gene can disrupt the normal functioning of the mitochondria, leading to a range of symptoms including muscle weakness, seizures, developmental delays, and vision and hearing loss.

NGS (Next Generation Sequencing) technology is used to analyze the MT-TR gene, which involves sequencing the DNA to identify any changes or mutations. This test can help to diagnose mitochondrial encephalomyopathy and provide information about the specific mutation present in the MT-TR gene. This information can be used to guide treatment and management of the condition.

Test Name MT-TR Gene Encephalomyopathy mitochondrial MT-TR 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 MT-TR Gene Encephalomyopathy, mitochondrial, MT-TR related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TR Gene Encephalomyopathy, mitochondrial, MT-TR related
Test Details

Encephalomyopathy, mitochondrial, MT-TR related NGS genetic test is a type of genetic testing that analyzes the MT-TR gene for mutations that may cause mitochondrial encephalomyopathy. Mitochondrial encephalomyopathy is a rare genetic disorder that affects the brain and muscles. The MT-TR gene provides instructions for making a protein called mitochondrial transfer RNA, which is involved in the production of energy within cells. Mutations in the MT-TR gene can disrupt the normal functioning of the mitochondria, leading to a range of symptoms including muscle weakness, seizures, developmental delays, and vision and hearing loss.

NGS (Next Generation Sequencing) technology is used to analyze the MT-TR gene, which involves sequencing the DNA to identify any changes or mutations. This test can help to diagnose mitochondrial encephalomyopathy and provide information about the specific mutation present in the MT-TR gene. This information can be used to guide treatment and management of the condition.