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GCM2 Gene Hypoparathyroidism Familial Isolated Genetic Test Cost

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

-21%

The GCM2 gene, also known as glial cells missing homolog 2, plays a crucial role in the development and function of the parathyroid glands, which are essential for regulating calcium levels in the body. Mutations in the GCM2 gene can lead to hypoparathyroidism, a condition characterized by insufficient production of parathyroid hormone (PTH), resulting in low calcium levels in the blood. Familial isolated hypoparathyroidism is a form of the condition that is inherited in a genetic manner, specifically affecting families through generations.

To diagnose this genetic form of hypoparathyroidism, a specialized genetic test is available. This test involves analyzing the patient’s DNA to identify mutations in the GCM2 gene that are known to cause the condition. It’s a critical tool for confirming the diagnosis, understanding the genetic basis of the disorder, and facilitating appropriate management and treatment strategies for affected individuals and their families.

In the UAE, this specific genetic test for familial isolated hypoparathyroidism caused by GCM2 gene mutations is offered by DNA Labs UAE. The cost of the test is 4400 AED. Conducting the test in a specialized facility like DNA Labs UAE ensures accuracy and reliability of the results, which are essential for the effective management of the condition. This test is particularly valuable for families with a history of hypoparathyroidism, as it can help in identifying at-risk family members and in making informed decisions regarding their health and management of the condition.

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GCM2 Gene Hypoparathyroidism familial isolated Genetic Test

At DNA Labs UAE, we offer the GCM2 Gene Hypoparathyroidism familial isolated Genetic Test at a cost of AED 4400.0.

Test Details

The GCM2 gene is associated with a condition called familial isolated hypoparathyroidism. This disorder is characterized by low levels of parathyroid hormone (PTH), which leads to low levels of calcium in the blood.

Familial isolated hypoparathyroidism refers to cases where the condition is inherited in a non-syndromic manner, meaning it is not associated with other developmental abnormalities or medical conditions.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of familial isolated hypoparathyroidism, NGS genetic testing can be used to identify mutations or variations in the GCM2 gene that may be causing the condition.

By analyzing the GCM2 gene, NGS genetic testing can help confirm a diagnosis of familial isolated hypoparathyroidism and identify specific genetic variants that are responsible for the condition.

This information can be useful for genetic counseling, family planning, and potentially guiding treatment decisions.

It is important to note that genetic testing for familial isolated hypoparathyroidism is typically performed in conjunction with a comprehensive clinical evaluation, including assessment of symptoms, family history, and other laboratory tests.

The results of genetic testing should be interpreted by a healthcare professional with expertise in genetics.

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: Hepatology Nephrology Endocrinology Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for GCM2 Gene Hypoparathyroidism, familial isolated NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GCM2 Gene Hypoparathyroidism, familial isolated NGS Genetic DNA Test gene GCM2.

Test Name GCM2 Gene Hypoparathyroidism familial isolated 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for GCM2 Gene Hypoparathyroidism, familial isolated NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GCM2 Gene Hypoparathyroidism, familial isolated NGS Genetic DNA Test gene GCM2
Test Details

The GCM2 gene is associated with a condition called familial isolated hypoparathyroidism. Hypoparathyroidism is a disorder characterized by low levels of parathyroid hormone (PTH), which leads to low levels of calcium in the blood.

Familial isolated hypoparathyroidism refers to cases where the condition is inherited in a non-syndromic manner, meaning it is not associated with other developmental abnormalities or medical conditions.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of familial isolated hypoparathyroidism, NGS genetic testing can be used to identify mutations or variations in the GCM2 gene that may be causing the condition.

By analyzing the GCM2 gene, NGS genetic testing can help confirm a diagnosis of familial isolated hypoparathyroidism and identify specific genetic variants that are responsible for the condition. This information can be useful for genetic counseling, family planning, and potentially guiding treatment decisions.

It is important to note that genetic testing for familial isolated hypoparathyroidism is typically performed in conjunction with a comprehensive clinical evaluation, including assessment of symptoms, family history, and other laboratory tests. The results of genetic testing should be interpreted by a healthcare professional with expertise in genetics.

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