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MT-ND3 Gene Mitochondrial Complex I Deficiency Genetic Test

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

-21%

The MT-ND3 gene mitochondrial complex I deficiency genetic test is a specialized diagnostic procedure aimed at detecting mutations in the MT-ND3 gene, which is crucial for the normal function of mitochondrial complex I. Mitochondrial complex I is a vital component of the mitochondrial respiratory chain, responsible for energy production within cells. Mutations in the MT-ND3 gene can lead to mitochondrial complex I deficiency, a condition that affects various body systems, particularly the nervous system and muscles, leading to a wide range of clinical manifestations from mild to severe.

This genetic test involves analyzing the patient’s DNA to identify mutations in the MT-ND3 gene, providing crucial information for the diagnosis, prognosis, and management of the condition. Early detection through this test can enable timely intervention and management strategies to mitigate the symptoms and improve the quality of life for affected individuals.

The test is available at DNA Labs UAE, a leading facility in genetic diagnostics, ensuring high-quality testing and reliable results. The cost of the MT-ND3 gene mitochondrial complex I deficiency genetic test is 4400 AED. Patients seeking this test can expect professional service, including pre-test counseling, efficient sample collection, and post-test guidance to understand their results and the implications for their health and potential treatment options.

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MT-ND3 Gene Mitochondrial complex I deficiency Genetic Test

At DNA Labs UAE, we offer the MT-ND3 Gene Mitochondrial complex I deficiency Genetic Test for individuals suspected to have mitochondrial complex I deficiency. This genetic test analyzes the MT-ND3 gene, which is responsible for encoding a subunit of the mitochondrial complex I enzyme.

Test Components and Price

The cost of the MT-ND3 Gene Mitochondrial complex I deficiency Genetic Test is AED 4400.0. The test requires a blood sample or extracted DNA. Alternatively, one drop of blood can be collected on an FTA card.

Report Delivery

After the sample is received, the report will be delivered within 3 to 4 weeks.

Testing Method

The MT-ND3 Gene Mitochondrial complex I deficiency Genetic Test utilizes NGS (Next-Generation Sequencing) technology. This advanced sequencing method allows for the simultaneous analysis of multiple genes.

Test Type

The MT-ND3 Gene Mitochondrial complex I deficiency Genetic Test is specifically designed to diagnose neurological disorders.

Referring Doctor and Test Department

This test is recommended for individuals who have been referred by a neurologist. The test is conducted in the Genetics department of DNA Labs UAE.

Pre Test Information

Prior to the test, a clinical history of the patient is required. This information helps in understanding the patient’s symptoms and medical background. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by MT-ND3 Gene Mitochondrial complex I deficiency.

Test Details

The MT-ND3 gene is a crucial component of the mitochondrial DNA (mtDNA) and is responsible for the production of ATP, which is essential for cellular energy. A deficiency in the MT-ND3 gene can lead to mitochondrial complex I deficiency, a rare genetic disorder. This deficiency affects the normal functioning of the electron transport chain and reduces ATP production.

Individuals with mitochondrial complex I deficiency may experience various symptoms, including muscle weakness, exercise intolerance, developmental delay, intellectual disability, seizures, and organ dysfunction.

The NGS genetic testing method used in this test allows for the identification of mutations or variations in the MT-ND3 gene and other genes associated with mitochondrial complex I deficiency. This testing helps confirm a diagnosis, identify the specific genetic cause of the disorder, and guide treatment options and genetic counseling.

Test Name MT-ND3 Gene Mitochondrial complex I deficiency 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-ND3 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ND3 Gene Mitochondrial complex I deficiency
Test Details

The MT-ND3 gene is a gene found in the mitochondrial DNA (mtDNA) and encodes for a subunit of the mitochondrial complex I enzyme. Mitochondrial complex I is responsible for the first step in the electron transport chain, which is crucial for the production of ATP (cellular energy).

A deficiency in the MT-ND3 gene can lead to mitochondrial complex I deficiency, which is a rare genetic disorder. This deficiency impairs the normal functioning of the electron transport chain and reduces the production of ATP. As a result, affected individuals may experience a wide range of symptoms, including muscle weakness, exercise intolerance, developmental delay, intellectual disability, seizures, and organ dysfunction.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations or variations in the MT-ND3 gene and other genes associated with mitochondrial complex I deficiency. This testing can help in confirming a diagnosis, identifying the specific genetic cause of the disorder, and guiding treatment options and genetic counseling.