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GFM1 Gene Combined oxidative phosphorylation deficiency type 1 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 3,200 د.إ.

-43%

The GFM1 gene plays a crucial role in the process of oxidative phosphorylation, a vital mechanism for energy production within cells. Mutations in the GFM1 gene can lead to combined oxidative phosphorylation deficiency type 1, a rare genetic disorder that affects multiple systems in the body, leading to severe clinical manifestations, including lactic acidosis, neurological deficits, and failure to thrive.

The genetic test for identifying mutations in the GFM1 gene is a critical tool for diagnosing combined oxidative phosphorylation deficiency type 1. This test involves analyzing the patient’s DNA to look for specific alterations in the GFM1 gene that are known to cause the disorder. Early diagnosis through genetic testing is essential for managing symptoms, implementing appropriate treatments, and providing genetic counseling to affected families.

In the UAE, DNA Labs offers this specialized genetic test for the GFM1 gene. The test cost is set at 3200 AED, reflecting the intricate processes and sophisticated technology involved in accurately detecting mutations within the gene. By choosing DNA Labs UAE for this test, patients and healthcare providers can expect reliable results, which are crucial for making informed decisions regarding the management of combined oxidative phosphorylation deficiency type 1.

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GFM1 Gene Combined Oxidative Phosphorylation Deficiency Type 1 Genetic Test

At DNA Labs UAE, we offer the GFM1 Gene Combined Oxidative Phosphorylation Deficiency Type 1 Genetic Test at a cost of AED 3200.0.

Test Details

The GFM1 Gene Combined Oxidative Phosphorylation Deficiency Type 1 Genetic Test is a type of genetic test that analyzes the GFM1 gene for mutations or variations associated with combined oxidative phosphorylation deficiency type 1. This rare genetic disorder is characterized by impaired energy production in the cells due to defects in the oxidative phosphorylation process.

The GFM1 gene provides instructions for making a protein called mitochondrial translation elongation factor G1 (EF-G1), which is involved in the synthesis of proteins within the mitochondria. The Next-Generation Sequencing (NGS) technology used in this genetic test allows for the simultaneous analysis of multiple genes, including the GFM1 gene, to identify any potential variations or mutations that may be causing the disorder.

This test can help in confirming a diagnosis, predicting disease progression, and guiding treatment options for individuals suspected to have combined oxidative phosphorylation deficiency type 1.

Test Components and Price

  • Test Name: GFM1 Gene Combined Oxidative Phosphorylation Deficiency Type 1 Genetic Test
  • Components: Blood or Extracted DNA or One drop Blood on FTA Card
  • Price: 3200.0 AED

Report Delivery

The report for the GFM1 Gene Combined Oxidative Phosphorylation Deficiency Type 1 Genetic Test will be delivered within 3 to 4 weeks.

Test Method

The GFM1 Gene Combined Oxidative Phosphorylation Deficiency Type 1 Genetic Test is conducted using NGS technology.

Test Type

This genetic test falls under the category of Metabolic Disorders.

Referring Doctor

This test can be referred by a General Physician.

Test Department

The GFM1 Gene Combined Oxidative Phosphorylation Deficiency Type 1 Genetic Test is conducted in the Genetics department.

Pre-Test Information

Prior to the test, it is important to provide the clinical history of the patient who is going for the GFM1 Gene Combined Oxidative Phosphorylation Deficiency Type 1 NGS Genetic DNA Test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with Combined Oxidative Phosphorylation Deficiency Type 1.

It is crucial to note that this genetic test should be performed and interpreted by a qualified healthcare professional or genetic counselor, as they can provide the necessary guidance and counseling regarding the implications of the test results and any further actions that may be required.

Test Name GFM1 Gene Combined oxidative phosphorylation deficiency type 1 Genetic Test
Components
Price 3200.0 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 GFM1 Gene Combined oxidative phosphorylation deficiency type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Combined oxidative phosphorylation deficiency type 1
Test Details

GFM1 gene combined oxidative phosphorylation deficiency type 1 NGS genetic test is a type of genetic test that analyzes the GFM1 gene for mutations or variations associated with combined oxidative phosphorylation deficiency type 1.

Combined oxidative phosphorylation deficiency type 1 is a rare genetic disorder characterized by impaired energy production in the cells due to defects in the oxidative phosphorylation process. The GFM1 gene provides instructions for making a protein called mitochondrial translation elongation factor G1 (EF-G1), which is involved in the synthesis of proteins within the mitochondria.

The NGS (Next-Generation Sequencing) technology used in this genetic test allows for the simultaneous analysis of multiple genes, including the GFM1 gene, to identify any potential variations or mutations that may be causing the disorder. This test can help in confirming a diagnosis, predicting disease progression, and guiding treatment options for individuals suspected to have combined oxidative phosphorylation deficiency type 1.

It is important to note that this genetic test should be performed and interpreted by a qualified healthcare professional or genetic counselor, as they can provide the necessary guidance and counseling regarding the implications of the test results and any further actions that may be required.