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CASR Gene Hyperparathyroidism Neonatal Severe Genetic Test

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

-21%

The CASR Gene Hyperparathyroidism Neonatal Severe Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the CASR gene, which are associated with neonatal severe hyperparathyroidism (NSHPT). NSHPT is a rare, inherited disorder characterized by abnormally high levels of calcium in the blood due to overactivity of the parathyroid glands. This condition can lead to severe complications, including skeletal demineralization and failure to thrive, making early detection and management crucial.

Performed at DNA Labs UAE, this test involves analyzing the patient’s DNA to identify any genetic alterations in the CASR gene that may predispose infants to this life-threatening condition. The CASR gene plays a critical role in regulating calcium levels in the body, and mutations in this gene can disrupt this balance, leading to NSHPT.

The cost of the CASR Gene Hyperparathyroidism Neonatal Severe Genetic Test is 4400 AED. Given the complexity and the specialized nature of this test, it represents a vital investment in the health and well-being of affected newborns, allowing for prompt and targeted treatment interventions. This test is an essential tool for parents with a family history of the condition or those whose newborns exhibit symptoms indicative of hyperparathyroidism, ensuring that affected infants receive the necessary care and treatment to mitigate the risks associated with this genetic disorder.

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CASR Gene Hyperparathyroidism Neonatal Severe Genetic Test

Components

  • Test Name: CASR Gene Hyperparathyroidism Neonatal Severe 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: Hepatology Nephrology Endocrinology Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for CASR Gene Hyperparathyroidism, neonatal severe NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CASR Gene Hyperparathyroidism, neonatal severe NGS Genetic DNA Test gene CASR.

Test Details

CASR gene hyperparathyroidism, neonatal severe is a genetic disorder that affects the function of the parathyroid glands. The CASR gene provides instructions for making a protein called the calcium-sensing receptor, which is involved in regulating the levels of calcium in the body.

Individuals with CASR gene hyperparathyroidism, neonatal severe have mutations in the CASR gene that impair the function of the calcium-sensing receptor. This leads to abnormally high levels of calcium in the blood, a condition known as hypercalcemia.

The excessive calcium levels can cause a variety of symptoms, including poor feeding, vomiting, dehydration, constipation, failure to thrive, and kidney problems.

NGS (Next Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of CASR gene hyperparathyroidism, neonatal severe, NGS genetic testing can be used to identify mutations in the CASR gene that are responsible for the condition.

This testing can help confirm a diagnosis and guide appropriate treatment and management options. It is important to note that genetic testing for CASR gene hyperparathyroidism, neonatal severe is typically recommended for individuals with symptoms suggestive of the condition, a family history of the disorder, or for prenatal testing in families with a known CASR gene mutation.

Genetic counseling is also often recommended before and after genetic testing to discuss the implications and potential outcomes of the test results.

Test Name CASR Gene Hyperparathyroidism neonatal severe 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 CASR Gene Hyperparathyroidism, neonatal severe NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CASR Gene Hyperparathyroidism, neonatal severe NGS Genetic DNA Test gene CASR
Test Details

CASR gene hyperparathyroidism, neonatal severe is a genetic disorder that affects the function of the parathyroid glands. The CASR gene provides instructions for making a protein called the calcium-sensing receptor, which is involved in regulating the levels of calcium in the body.

Individuals with CASR gene hyperparathyroidism, neonatal severe have mutations in the CASR gene that impair the function of the calcium-sensing receptor. This leads to abnormally high levels of calcium in the blood, a condition known as hypercalcemia. The excessive calcium levels can cause a variety of symptoms, including poor feeding, vomiting, dehydration, constipation, failure to thrive, and kidney problems.

NGS (Next Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of CASR gene hyperparathyroidism, neonatal severe, NGS genetic testing can be used to identify mutations in the CASR gene that are responsible for the condition. This testing can help confirm a diagnosis and guide appropriate treatment and management options.

It is important to note that genetic testing for CASR gene hyperparathyroidism, neonatal severe is typically recommended for individuals with symptoms suggestive of the condition, a family history of the disorder, or for prenatal testing in families with a known CASR gene mutation. Genetic counseling is also often recommended before and after genetic testing to discuss the implications and potential outcomes of the test results.

SKU: TEST-3656 Category:

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