CYP2R1 Gene Rickets Vitamin D 25-Hydroxylation-Deficient Type 1B Genetic Test
Are you or your family members experiencing symptoms of rickets? DNA Labs UAE offers the CYP2R1 Gene Rickets Vitamin D 25-Hydroxylation-Deficient Type 1B Genetic Test to help diagnose and manage this condition. Read on to learn more about the test, its components, cost, symptoms, diagnosis, and more.
Test Name: CYP2R1 Gene Rickets Vitamin D 25-Hydroxylation-Deficient Type 1B 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:
Prior to undergoing the CYP2R1 Gene Rickets Vitamin D 25-Hydroxylation-Deficient Type 1B Genetic Test, it is important to provide the clinical history of the patient. A genetic counseling session will be conducted to draw a pedigree chart of family members affected by CYP2R1 Gene Rickets Vitamin D 25-Hydroxylation-Deficient Type 1B NGS Genetic DNA Test gene CYP2R1.
Test Details:
The CYP2R1 gene is responsible for encoding an enzyme called cytochrome P450 2R1. This enzyme plays a crucial role in the metabolism of vitamin D. Mutations in the CYP2R1 gene can lead to a condition called rickets, specifically vitamin D 25-hydroxylation-deficient type 1B.
Rickets is a disorder characterized by impaired bone growth and development, primarily caused by a deficiency in vitamin D. Vitamin D is essential for the absorption of calcium and phosphorus from the intestine, which are necessary for proper bone mineralization.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic analysis that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of rickets, an NGS genetic test can be used to identify mutations in the CYP2R1 gene, providing a molecular diagnosis for vitamin D 25-hydroxylation-deficient type 1B.
This genetic test involves obtaining a DNA sample, typically through a blood sample or saliva swab, and analyzing the DNA sequence of the CYP2R1 gene using NGS technology. By identifying specific mutations in the gene, healthcare professionals can confirm a diagnosis of vitamin D 25-hydroxylation-deficient type 1B and provide appropriate management and treatment options for the patient.
Don’t let rickets go undiagnosed. Contact DNA Labs UAE today to schedule your CYP2R1 Gene Rickets Vitamin D 25-Hydroxylation-Deficient Type 1B Genetic Test and take control of your health.
| Test Name | CYP2R1 Gene Rickets vitamin D 25-hydroxylation-deficient type 1B 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 CYP2R1 Gene Rickets, vitamin D 25-hydroxylation-deficient, type 1B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYP2R1 Gene Rickets, vitamin D 25-hydroxylation-deficient, type 1B NGS Genetic DNA Test gene CYP2R1 |
| Test Details |
The CYP2R1 gene is responsible for encoding an enzyme called cytochrome P450 2R1, which plays a crucial role in the metabolism of vitamin D. Mutations in the CYP2R1 gene can lead to a condition called rickets, specifically vitamin D 25-hydroxylation-deficient type 1B. Rickets is a disorder characterized by impaired bone growth and development, primarily caused by a deficiency in vitamin D. Vitamin D is essential for the absorption of calcium and phosphorus from the intestine, which are necessary for proper bone mineralization. NGS (Next-Generation Sequencing) genetic testing is a type of genetic analysis that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of rickets, an NGS genetic test can be used to identify mutations in the CYP2R1 gene, providing a molecular diagnosis for vitamin D 25-hydroxylation-deficient type 1B. This genetic test involves obtaining a DNA sample, typically through a blood sample or saliva swab, and analyzing the DNA sequence of the CYP2R1 gene using NGS technology. By identifying specific mutations in the gene, healthcare professionals can confirm a diagnosis of vitamin D 25-hydroxylation-deficient type 1B and provide appropriate management and treatment options for the patient. |
