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. |
