SLC34A3 Gene Hypophosphatemic rickets with hypercalciuria Genetic Test
At DNA Labs UAE, we offer the SLC34A3 Gene Hypophosphatemic rickets with hypercalciuria Genetic Test at a cost of AED 4400.0. This test is used to diagnose and identify mutations or variations in the SLC34A3 gene that may be responsible for hypophosphatemic rickets with hypercalciuria (HRH).
Test Details
The SLC34A3 gene is associated with HRH, a rare genetic disorder characterized by low levels of phosphate in the blood (hypophosphatemia) and increased levels of calcium in the urine (hypercalciuria). This condition leads to impaired bone mineralization, resulting in rickets.
Our SLC34A3 Gene Hypophosphatemic rickets with hypercalciuria Genetic Test utilizes NGS (Next-Generation Sequencing) technology, which allows us to analyze multiple genes simultaneously. By identifying specific genetic changes in the SLC34A3 gene, this test can help confirm a diagnosis of HRH and provide valuable information for medical management and genetic counseling.
Additionally, the test can determine the mode of inheritance and assess the risk of passing the condition on to future generations.
Test Components and Price
The SLC34A3 Gene Hypophosphatemic rickets with hypercalciuria Genetic Test costs AED 4400.0.
Sample Condition
We accept blood or extracted DNA samples for this test. Alternatively, one drop of blood can be collected on an FTA card.
Report Delivery
The report will be delivered within 3 to 4 weeks after sample collection.
Test Type and Department
The SLC34A3 Gene Hypophosphatemic rickets with hypercalciuria Genetic Test falls under the category of Osteology Dermatology Immunology Disorders and is conducted by our Genetics department.
Pre Test Information
Before undergoing the SLC34A3 Gene Hypophosphatemic rickets with hypercalciuria Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by HRH.
Doctor and Referring
This test is referred by a Dermatologist.
For more information or to schedule an appointment, please contact our Genetics department.
| Test Name | SLC34A3 Gene Hypophosphatemic rickets with hypercalciuria 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 | Osteology Dermatology Immunology Disorders |
| Doctor | Dermatologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for SLC34A3 Gene Hypophosphatemic rickets with hypercalciuria NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC34A3 Gene Hypophosphatemic rickets with hypercalciuria NGS Genetic DNA Test gene SLC34A3 |
| Test Details |
The SLC34A3 gene is associated with a condition called hypophosphatemic rickets with hypercalciuria (HRH). HRH is a rare genetic disorder characterized by low levels of phosphate in the blood (hypophosphatemia) and increased levels of calcium in the urine (hypercalciuria). This condition leads to impaired bone mineralization, resulting in rickets. NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of HRH, NGS genetic testing can be used to identify mutations or variations in the SLC34A3 gene that may be responsible for the development of the condition. By identifying specific genetic changes in the SLC34A3 gene, NGS genetic testing can help confirm a diagnosis of HRH and provide valuable information for medical management and genetic counseling. It can also help determine the mode of inheritance and assess the risk of passing the condition on to future generations. |
