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EGF Gene Hypomagnesemia Type 4 Genetic Test Cost

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

-21%

The “EGF Gene Hypomagnesemia Type 4 Genetic Test” is a specialized diagnostic procedure aimed at identifying mutations in the EGF gene, which are linked to Hypomagnesemia Type 4, a rare genetic disorder. This condition is characterized by abnormally low levels of magnesium in the blood, which can lead to a variety of health issues, including muscle spasms, seizures, and cardiac abnormalities. Early detection through this genetic test is crucial for the management and treatment of the disorder.

The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the test is 4400 AED, reflecting the intricate technologies and expertise required to accurately identify mutations in the EGF gene. This test is essential for individuals with a family history of Hypomagnesemia or those exhibiting symptoms of magnesium deficiency, as it provides a definitive diagnosis, enabling targeted treatment strategies to manage the condition effectively.

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EGF Gene Hypomagnesemia type 4 Genetic Test

Are you concerned about Hypomagnesemia type 4? DNA Labs UAE offers the EGF Gene Hypomagnesemia type 4 Genetic Test to help diagnose this rare genetic disorder. Read on to learn more about the test.

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 and Test Department

This test can be ordered by a General Physician and is conducted in the Genetics department.

Pre Test Information

Prior to the test, a Genetic Counselling session is recommended. This session will help draw a pedigree chart of family members affected with Hypomagnesemia type 4, providing valuable information for the test.

Test Details

The EGF Gene Hypomagnesemia type 4 NGS Genetic Test utilizes next-generation sequencing (NGS) technology to analyze the EGF gene for mutations associated with Hypomagnesemia type 4. Hypomagnesemia type 4 is a rare genetic disorder characterized by low levels of magnesium in the blood.

The EGF gene is responsible for producing a protein called epidermal growth factor (EGF), which plays a role in regulating magnesium levels in the body. Mutations in the EGF gene can disrupt the normal functioning of this protein, leading to Hypomagnesemia type 4.

The NGS genetic test involves sequencing the DNA of an individual to identify any variations or mutations in the EGF gene. This comprehensive test can help diagnose individuals with Hypomagnesemia type 4 and guide appropriate treatment and management strategies.

NGS technology allows for the analysis of multiple genes simultaneously, providing a comprehensive assessment of genetic variations that may contribute to the condition. This approach increases the efficiency and accuracy of genetic testing compared to traditional methods.

The EGF Gene Hypomagnesemia type 4 NGS Genetic Test is a valuable tool for identifying genetic mutations in the EGF gene associated with Hypomagnesemia type 4, enabling early diagnosis and personalized treatment for affected individuals.

Test Name EGF Gene Hypomagnesemia type 4 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 EGF Gene Hypomagnesemia type 4 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hypomagnesemia type 4
Test Details

EGF Gene Hypomagnesemia type 4 NGS Genetic Test is a genetic test that uses next-generation sequencing (NGS) technology to analyze the EGF gene for mutations associated with Hypomagnesemia type 4. Hypomagnesemia type 4 is a rare genetic disorder characterized by low levels of magnesium in the blood.

The EGF gene provides instructions for producing a protein called epidermal growth factor (EGF), which plays a role in various cellular processes, including the regulation of magnesium levels in the body. Mutations in the EGF gene can disrupt the normal functioning of this protein, leading to Hypomagnesemia type 4.

The NGS genetic test involves sequencing the DNA of an individual to identify any variations or mutations in the EGF gene. This test can help diagnose individuals with Hypomagnesemia type 4 and guide appropriate treatment and management strategies.

NGS technology allows for the analysis of multiple genes simultaneously, providing a comprehensive assessment of genetic variations that may contribute to the condition. This approach increases the efficiency and accuracy of genetic testing compared to traditional methods.

Overall, the EGF Gene Hypomagnesemia type 4 NGS Genetic Test is a valuable tool for identifying genetic mutations in the EGF gene associated with Hypomagnesemia type 4, enabling early diagnosis and personalized treatment for affected individuals.

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