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CASR Gene Hypocalciuric Hypercalcemia Type 1 Genetic Test Cost

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

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The CASR Gene Hypocalciuric Hypercalcemia Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the CASR gene, which are implicated in the development of Hypocalciuric Hypercalcemia Type 1. This condition is characterized by elevated levels of calcium in the blood, yet with low levels of calcium excreted in the urine, a phenomenon that can lead to various health issues including kidney stones, cognitive disorders, and bone abnormalities.

The test is crucial for individuals with a family history of the condition or those exhibiting symptoms, as early detection can lead to better management and treatment strategies. Conducted through a simple blood sample, the test examines the CASR gene for specific mutations, providing insights that are vital for accurate diagnosis and guiding therapeutic decisions.

Priced at 4400 AED, the test represents a significant investment in personal health, offering a window into the genetic underpinnings of Hypocalciuric Hypercalcemia Type 1. DNA Labs UAE, with its state-of-the-art facilities and expert staff, ensures a reliable, accurate, and confidential testing process, making it a trusted choice for genetic testing services in the region.

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CASR Gene Hypocalciuric Hypercalcemia Type 1 Genetic Test

Introduction

CASR gene hypocalciuric hypercalcemia, type 1 is a genetic disorder characterized by high levels of calcium in the blood (hypercalcemia) and low levels of calcium in the urine (hypocalciuria). It is caused by mutations in the CASR gene, which provides instructions for making a protein called the calcium-sensing receptor. This receptor is involved in regulating the amount of calcium in the body.

Test Details

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. It allows for the rapid and efficient analysis of large amounts of genetic data, making it a useful tool for diagnosing genetic disorders like CASR gene hypocalciuric hypercalcemia, type 1.

NGS genetic testing for CASR gene hypocalciuric hypercalcemia, type 1 involves sequencing the CASR gene to identify any mutations or variations that may be causing the disorder. This can help confirm a diagnosis, guide treatment decisions, and provide information about the inheritance pattern of the condition.

Test Components and Price

Test Name: CASR Gene Hypocalciuric Hypercalcemia Type 1 Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition

Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery

3 to 4 Weeks

Test Type

Hepatology, Nephrology, Endocrinology Disorders

Referring Doctor

General Physician

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for CASR Gene Hypocalciuric Hypercalcemia, type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CASR Gene Hypocalciuric Hypercalcemia, type 1 NGS Genetic DNA Test gene CASR.

Conclusion

If you suspect you or someone you know may have CASR gene hypocalciuric hypercalcemia, type 1, consulting with a healthcare professional or a genetic counselor is recommended. They can provide more information about the condition, help determine if genetic testing is appropriate, and assist in interpreting the results of the test.

Test Name CASR Gene Hypocalciuric hypercalcemia 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for CASR Gene Hypocalciuric hypercalcemia, type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CASR Gene Hypocalciuric hypercalcemia, type 1 NGS Genetic DNA Test gene CASR
Test Details

CASR gene hypocalciuric hypercalcemia, type 1 is a genetic disorder characterized by high levels of calcium in the blood (hypercalcemia) and low levels of calcium in the urine (hypocalciuria). It is caused by mutations in the CASR gene, which provides instructions for making a protein called the calcium-sensing receptor. This receptor is involved in regulating the amount of calcium in the body.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. It allows for the rapid and efficient analysis of large amounts of genetic data, making it a useful tool for diagnosing genetic disorders like CASR gene hypocalciuric hypercalcemia, type 1.

NGS genetic testing for CASR gene hypocalciuric hypercalcemia, type 1 involves sequencing the CASR gene to identify any mutations or variations that may be causing the disorder. This can help confirm a diagnosis, guide treatment decisions, and provide information about the inheritance pattern of the condition.

If you suspect you or someone you know may have CASR gene hypocalciuric hypercalcemia, type 1, consulting with a healthcare professional or a genetic counselor is recommended. They can provide more information about the condition, help determine if genetic testing is appropriate, and assist in interpreting the results of the test.

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