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FXYD2 Gene Hypomagnesemia Type 2 Genetic Test Cost

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

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The FXYD2 gene hypomagnesemia type 2 genetic test is a specialized diagnostic tool used to identify mutations in the FXYD2 gene, which are known to cause a specific type of inherited hypomagnesemia. Hypomagnesemia refers to abnormally low levels of magnesium in the blood, a condition that can lead to various health issues, including muscle weakness, seizures, and cardiac problems. Type 2 hypomagnesemia, linked to mutations in the FXYD2 gene, affects the kidney’s ability to retain magnesium, leading to its excessive loss in urine.

This genetic test involves analyzing the patient’s DNA to detect any abnormalities in the FXYD2 gene that could be responsible for the condition. It is a critical step for families with a history of hypomagnesemia, offering them valuable insights into their genetic predispositions and aiding in the early diagnosis and management of the condition in affected family members.

Performed at DNA Labs UAE, a leading facility in genetic testing, the test ensures high accuracy and reliability. The cost of the FXYD2 gene hypomagnesemia type 2 genetic test is set at 4400 AED. This investment covers the collection of the sample, usually a blood sample, the genetic analysis, and the comprehensive report detailing the findings. Given the specialized nature of this test and the profound implications of its results, it represents a critical tool in managing and understanding inherited hypomagnesemia, guiding both patients and healthcare providers in developing effective treatment and management plans.

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FXYD2 Gene Hypomagnesemia type 2 Genetic Test

Test Name: FXYD2 Gene Hypomagnesemia type 2 Genetic Test

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

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 FXYD2 Gene Hypomagnesemia type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Hypomagnesemia type 2.

Test Details

The FXYD2 gene is associated with a condition called hypomagnesemia type 2, which is characterized by low levels of magnesium in the blood. This condition can lead to various symptoms, including muscle cramps, seizures, and abnormal heart rhythms.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the analysis of multiple genes simultaneously. In the context of hypomagnesemia type 2, an NGS genetic test would involve sequencing the FXYD2 gene to identify any mutations or variations that may be causing the condition.

By identifying specific genetic variants in the FXYD2 gene, NGS testing can help diagnose hypomagnesemia type 2 and provide valuable information for treatment and management of the condition. It can also be used for genetic counseling and family planning purposes.

It’s important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals with expertise in genetics. They can provide guidance on the implications of the test results and help determine the best course of action for individuals and their families.

Test Name FXYD2 Gene Hypomagnesemia type 2 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 FXYD2 Gene Hypomagnesemia type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hypomagnesemia type 2
Test Details

The FXYD2 gene is associated with a condition called hypomagnesemia type 2, which is characterized by low levels of magnesium in the blood. This condition can lead to various symptoms, including muscle cramps, seizures, and abnormal heart rhythms.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the analysis of multiple genes simultaneously. In the context of hypomagnesemia type 2, an NGS genetic test would involve sequencing the FXYD2 gene to identify any mutations or variations that may be causing the condition.

By identifying specific genetic variants in the FXYD2 gene, NGS testing can help diagnose hypomagnesemia type 2 and provide valuable information for treatment and management of the condition. It can also be used for genetic counseling and family planning purposes.

It’s important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals with expertise in genetics. They can provide guidance on the implications of the test results and help determine the best course of action for individuals and their families.

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