CNNM2 Gene Hypomagnesemia Type 6 Genetic Test sale cost 4400 AED
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CNNM2 Gene Hypomagnesemia Type 6 Genetic Test Cost

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

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The CNNM2 Gene Hypomagnesemia Type 6 Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to detect mutations in the CNNM2 gene, which are linked to Type 6 Hypomagnesemia. This condition is characterized by abnormally low levels of magnesium in the blood, a crucial mineral that plays a vital role in numerous bodily functions, including muscle and nerve function, bone health, and regulating blood pressure. Mutations in the CNNM2 gene can disrupt the body’s ability to regulate magnesium levels properly, leading to a range of symptoms from muscle spasms and seizures to abnormal heart rhythms.

The test is crucial for individuals showing symptoms of magnesium deficiency or those with a family history of Type 6 Hypomagnesemia, as early detection can significantly aid in managing the condition. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed for specific genetic alterations in the CNNM2 gene.

The cost of the CNNM2 Gene Hypomagnesemia Type 6 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to identify the presence of any genetic mutations associated with the condition. Given the specialized nature of the test and the expertise required to interpret the results, the test price reflects the technical and professional services involved in providing accurate and actionable genetic insights.

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CNNM2 Gene Hypomagnesemia type 6 Genetic Test

Test Name: CNNM2 Gene Hypomagnesemia type 6 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 CNNM2 Gene Hypomagnesemia type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Hypomagnesemia type 6.

Test Details

The CNNM2 Gene Hypomagnesemia type 6 NGS Genetic Test is a type of genetic test that analyzes the CNNM2 gene for mutations or variations that may be associated with hypomagnesemia type 6. Hypomagnesemia is a condition characterized by low levels of magnesium in the blood, which can lead to various symptoms and health complications.

NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that allows for the rapid and efficient analysis of multiple genes or the entire genome. In the case of CNNM2 gene hypomagnesemia type 6 NGS genetic test, it means that the test uses NGS technology to analyze the CNNM2 gene for any mutations or variations that may be linked to hypomagnesemia type 6.

This type of genetic test can help in the diagnosis and management of individuals with suspected or confirmed hypomagnesemia type 6. By identifying specific genetic mutations or variations in the CNNM2 gene, healthcare professionals can provide personalized treatment and management strategies for affected individuals. It can also help in genetic counseling and family planning for individuals with a family history of hypomagnesemia type 6.

Test Name CNNM2 Gene Hypomagnesemia type 6 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 CNNM2 Gene Hypomagnesemia type 6 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hypomagnesemia type 6
Test Details

CNNM2 Gene Hypomagnesemia type 6 NGS Genetic Test is a type of genetic test that analyzes the CNNM2 gene for mutations or variations that may be associated with hypomagnesemia type 6. Hypomagnesemia is a condition characterized by low levels of magnesium in the blood, which can lead to various symptoms and health complications.

NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that allows for the rapid and efficient analysis of multiple genes or the entire genome. In the case of CNNM2 gene hypomagnesemia type 6 NGS genetic test, it means that the test uses NGS technology to analyze the CNNM2 gene for any mutations or variations that may be linked to hypomagnesemia type 6.

This type of genetic test can help in the diagnosis and management of individuals with suspected or confirmed hypomagnesemia type 6. By identifying specific genetic mutations or variations in the CNNM2 gene, healthcare professionals can provide personalized treatment and management strategies for affected individuals. It can also help in genetic counseling and family planning for individuals with a family history of hypomagnesemia type 6.

SKU: TEST-2475 Category:

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