FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant Genetic Test
Test Details:
FGF23 gene hypophosphatemic rickets, autosomal dominant is a rare genetic disorder characterized by low levels of phosphate in the blood, leading to soft and weak bones (rickets). This condition is caused by mutations in the FGF23 gene, which provides instructions for making a protein called fibroblast growth factor 23.
Autosomal dominant inheritance means that a person only needs to inherit one copy of the mutated gene from one parent to develop the condition. In other words, if one parent has the condition, there is a 50% chance of passing it on to each child.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of FGF23 gene hypophosphatemic rickets, autosomal dominant, NGS genetic testing can identify mutations in the FGF23 gene, confirming the diagnosis of the condition.
NGS genetic testing involves obtaining a DNA sample, typically through a blood sample or saliva sample. The DNA is then sequenced using advanced technology, allowing for the detection of mutations in the FGF23 gene. This information can help healthcare professionals provide appropriate management and treatment options for individuals with this 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:
Metabolic Disorders
Doctor:
General Physician
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 Hypophosphatemic Rickets, Autosomal Dominant.
| 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 | Metabolic Disorders |
| Doctor | General Physician |
| 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 Hypophosphatemic rickets, autosomal dominant |
| Test Details |
FGF23 gene hypophosphatemic rickets, autosomal dominant is a rare genetic disorder characterized by low levels of phosphate in the blood, leading to soft and weak bones (rickets). This condition is caused by mutations in the FGF23 gene, which provides instructions for making a protein called fibroblast growth factor 23. Autosomal dominant inheritance means that a person only needs to inherit one copy of the mutated gene from one parent to develop the condition. In other words, if one parent has the condition, there is a 50% chance of passing it on to each child. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of FGF23 gene hypophosphatemic rickets, autosomal dominant, NGS genetic testing can identify mutations in the FGF23 gene, confirming the diagnosis of the condition. NGS genetic testing involves obtaining a DNA sample, typically through a blood sample or saliva sample. The DNA is then sequenced using advanced technology, allowing for the detection of mutations in the FGF23 gene. This information can help healthcare professionals provide appropriate management and treatment options for individuals with this condition. |
