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TRPM6 Gene Hypomagnesemia Type 1 Genetic Test

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

-21%

The “TRPM6 Gene Hypomagnesemia Type 1 Genetic Test” is a specialized diagnostic procedure aimed at identifying mutations in the TRPM6 gene, which are known to cause Hypomagnesemia Type 1, a rare inherited condition characterized by low levels of magnesium in the blood. This condition can lead to various symptoms, including muscle spasms, seizures, and irregular heartbeats, making early diagnosis crucial for effective management and treatment.

Performed at DNA Labs UAE, this test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed to detect any genetic abnormalities in the TRPM6 gene. The process is highly sophisticated, requiring state-of-the-art technology and expertise in genetic analysis.

The cost of the TRPM6 Gene Hypomagnesemia Type 1 Genetic Test at DNA Labs UAE is 4400 AED. While the price might seem high, it reflects the complexity of the testing process and the invaluable insights it provides into managing and treating Hypomagnesemia Type 1. Early detection through this test can significantly improve the quality of life for individuals with this condition by enabling tailored treatment strategies and preventive measures.

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TRPM6 Gene Hypomagnesemia type 1 Genetic Test

Components: TRPM6 Gene Hypomagnesemia type 1 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 TRPM6 Gene Hypomagnesemia type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Hypomagnesemia type 1.

Test Details

TRPM6 gene hypomagnesemia type 1 NGS genetic test is a genetic test that examines the TRPM6 gene for mutations or variations that may cause hypomagnesemia type 1. Hypomagnesemia type 1 is a rare genetic disorder characterized by low levels of magnesium in the blood.

The TRPM6 gene provides instructions for making a protein that is involved in the absorption of magnesium from the intestines and its reabsorption in the kidneys. Mutations or variations in this gene can disrupt the normal functioning of the protein, leading to reduced magnesium levels in the body.

The NGS (Next-Generation Sequencing) genetic test is a high-throughput sequencing method that allows for the analysis of multiple genes simultaneously. In the case of TRPM6 gene hypomagnesemia type 1 NGS genetic test, it involves sequencing the TRPM6 gene to identify any mutations or variations that may be associated with the condition.

This genetic test can be used for diagnostic purposes to confirm a suspected case of hypomagnesemia type 1. It can also be used for carrier testing to identify individuals who carry a single copy of the mutated gene but do not show symptoms of the condition. Additionally, this test can be used for prenatal testing to determine if a fetus has inherited the mutated gene.

The results of the TRPM6 gene hypomagnesemia type 1 NGS genetic test can help healthcare providers make informed decisions regarding treatment, management, and genetic counseling for individuals with hypomagnesemia type 1 or those at risk of passing on the condition to their offspring.

Test Name TRPM6 Gene Hypomagnesemia type 1 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 TRPM6 Gene Hypomagnesemia type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hypomagnesemia type 1
Test Details

TRPM6 gene hypomagnesemia type 1 NGS genetic test is a genetic test that examines the TRPM6 gene for mutations or variations that may cause hypomagnesemia type 1.

Hypomagnesemia type 1 is a rare genetic disorder characterized by low levels of magnesium in the blood. The TRPM6 gene provides instructions for making a protein that is involved in the absorption of magnesium from the intestines and its reabsorption in the kidneys. Mutations or variations in this gene can disrupt the normal functioning of the protein, leading to reduced magnesium levels in the body.

The NGS (Next-Generation Sequencing) genetic test is a high-throughput sequencing method that allows for the analysis of multiple genes simultaneously. In the case of TRPM6 gene hypomagnesemia type 1 NGS genetic test, it involves sequencing the TRPM6 gene to identify any mutations or variations that may be associated with the condition.

This genetic test can be used for diagnostic purposes to confirm a suspected case of hypomagnesemia type 1. It can also be used for carrier testing to identify individuals who carry a single copy of the mutated gene but do not show symptoms of the condition. Additionally, this test can be used for prenatal testing to determine if a fetus has inherited the mutated gene.

The results of the TRPM6 gene hypomagnesemia type 1 NGS genetic test can help healthcare providers make informed decisions regarding treatment, management, and genetic counseling for individuals with hypomagnesemia type 1 or those at risk of passing on the condition to their offspring.

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