FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant Genetic Test
Welcome to DNA Labs UAE, where we offer the FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant Genetic Test. This test is designed to analyze the FGF23 gene and detect any mutations or variations that may be causing the condition known as hypophosphatemic rickets, autosomal dominant.
Test Details
The FGF23 gene is associated with hypophosphatemic rickets, autosomal dominant, a genetic condition characterized by low levels of phosphate in the blood. This can lead to weak and soft bones, also known as rickets, as well as other skeletal abnormalities.
Our FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant Genetic Test uses Next-Generation Sequencing (NGS) technology to analyze multiple genes simultaneously. By examining the FGF23 gene, we can identify any genetic abnormalities that may be causing the symptoms of hypophosphatemic rickets.
Test Components and Price
The FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA Card. The report will be delivered within 3 to 4 weeks.
Test Type and Method
This test falls under the categories of Osteology, Dermatology, and Immunology Disorders. It is performed by our expert Dermatologist in our Genetics Test Department. The NGS technology is utilized for accurate and comprehensive analysis.
Pre-Test Information
Prior to undergoing the FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant 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 the condition.
Interpreting the Results
It is crucial to note that the results of this test should be interpreted by a geneticist or a healthcare provider with expertise in genetics. They will be able to analyze the findings and provide a diagnosis, understand the underlying cause of the condition, and guide treatment decisions.
At DNA Labs UAE, we prioritize accuracy and professionalism in our genetic testing services. If you or a loved one are experiencing symptoms of hypophosphatemic rickets, autosomal dominant, consider our FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant Genetic Test to gain valuable insights into your condition.
| Test Name | FGF23 Gene Hypophosphatemic rickets autosomal dominant 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 FGF23 Gene Hypophosphatemic rickets, autosomal dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGF23 Gene Hypophosphatemic rickets, autosomal dominant NGS Genetic DNA Test gene FGF23 |
| Test Details |
The FGF23 gene is associated with a genetic condition called hypophosphatemic rickets, autosomal dominant. This condition is characterized by low levels of phosphate in the blood, leading to weak and soft bones (rickets) and other skeletal abnormalities. 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 case of hypophosphatemic rickets, autosomal dominant, NGS genetic testing can be used to identify mutations or variations in the FGF23 gene that may be causing the condition. By analyzing the FGF23 gene using NGS technology, healthcare providers can determine if there are any genetic abnormalities present that may be causing the symptoms of hypophosphatemic rickets. This information can be helpful in making a diagnosis, understanding the underlying cause of the condition, and guiding treatment decisions. It’s important to note that NGS genetic testing for hypophosphatemic rickets, autosomal dominant is typically performed by a healthcare professional or a specialized genetic testing laboratory. The results of the test should be interpreted by a geneticist or a healthcare provider with expertise in genetics. |
