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MPC1 Gene Mitochondrial Pyruvate Carrier Deficiency Genetic Test Cost

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

-21%

The MPC1 Gene Mitochondrial Pyruvate Carrier Deficiency Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the MPC1 gene, which can lead to mitochondrial pyruvate carrier deficiency. This condition is rare and affects how the body converts food into energy, leading to a range of metabolic problems. The test is crucial for early detection and management of the disorder, ensuring patients receive appropriate care and interventions.

At a cost of 4400 AED, the test is conducted using advanced genetic sequencing technologies to analyze the MPC1 gene for any abnormalities or mutations that may interfere with the normal function of the mitochondrial pyruvate carrier. This carrier is essential for transporting pyruvate into mitochondria, where it plays a key role in energy production. A deficiency can result in a wide array of symptoms, including developmental delay, muscle weakness, and metabolic crises, making early and accurate diagnosis vital.

DNA Labs UAE is equipped with state-of-the-art facilities and staffed by expert geneticists and clinicians who specialize in metabolic and genetic disorders. Their comprehensive approach ensures not only the accuracy of the test but also provides support and guidance for affected individuals and their families, including counseling and recommendations for treatment and management strategies following a diagnosis.

Description

MPC1 Gene Mitochondrial pyruvate carrier deficiency Genetic Test

Components: MPC1 Gene Mitochondrial pyruvate carrier deficiency Genetic Test

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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for MPC1 Gene Mitochondrial pyruvate carrier deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Mitochondrial pyruvate carrier deficiency.

Test Details: The MPC1 gene is responsible for encoding a protein that is involved in the transport of pyruvate into the mitochondria. Mitochondrial pyruvate carrier deficiency is a rare genetic disorder that is caused by mutations in the MPC1 gene, leading to impaired pyruvate transport and subsequent dysfunction of the mitochondria. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of mitochondrial pyruvate carrier deficiency, NGS genetic testing can be used to identify mutations in the MPC1 gene, helping to confirm a diagnosis of the disorder. NGS genetic testing is a powerful tool for diagnosing genetic disorders, as it allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of an individual’s genetic makeup. This can help to identify the specific genetic cause of a disorder, allowing for more accurate diagnosis, prognosis, and personalized treatment options.

Test Name	MPC1 Gene Mitochondrial pyruvate carrier deficiency 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	Metabolic Disorders
Doctor	General Physician
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for MPC1 Gene Mitochondrial pyruvate carrier deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Mitochondrial pyruvate carrier deficiency
Test Details	The MPC1 gene is responsible for encoding a protein that is involved in the transport of pyruvate into the mitochondria. Mitochondrial pyruvate carrier deficiency is a rare genetic disorder that is caused by mutations in the MPC1 gene, leading to impaired pyruvate transport and subsequent dysfunction of the mitochondria. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of mitochondrial pyruvate carrier deficiency, NGS genetic testing can be used to identify mutations in the MPC1 gene, helping to confirm a diagnosis of the disorder. NGS genetic testing is a powerful tool for diagnosing genetic disorders, as it allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of an individual’s genetic makeup. This can help to identify the specific genetic cause of a disorder, allowing for more accurate diagnosis, prognosis, and personalized treatment options.