DGKE Gene Nephrotic Syndrome Type 7 Genetic Test
Components
- Test Name: DGKE Gene Nephrotic syndrome type 7 Genetic Test
- 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 DGKE Gene Nephrotic syndrome type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DGKE Gene Nephrotic syndrome type 7 NGS Genetic DNA Test gene DGKE.
Test Details
The DGKE gene is associated with Nephrotic Syndrome Type 7 (NPHS7), also known as phospholipase C epsilon 1 deficiency. NPHS7 is a rare genetic disorder characterized by proteinuria (excessive protein in the urine), nephrotic syndrome (a kidney disorder), and chronic kidney disease.
NGS (Next-Generation Sequencing) genetic testing refers to a high-throughput DNA sequencing technology that can analyze multiple genes simultaneously. In the context of NPHS7, NGS genetic testing can be used to identify mutations or variants in the DGKE gene that may be responsible for the development of the disease.
NGS genetic testing for NPHS7 can help with accurate diagnosis, genetic counseling, and management of individuals with suspected or confirmed NPHS7. It can also assist in identifying family members who may be at risk of inheriting the condition.
It is important to note that NGS genetic testing for NPHS7 is typically performed by specialized laboratories and should be ordered and interpreted by healthcare professionals with expertise in genetics. Genetic counseling is also recommended to discuss the implications of the test results and the inheritance pattern of NPHS7.
| Test Name | DGKE Gene Nephrotic syndrome type 7 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 DGKE Gene Nephrotic syndrome type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DGKE Gene Nephrotic syndrome type 7 NGS Genetic DNA Test gene DGKE |
| Test Details | The DGKE gene is associated with Nephrotic Syndrome Type 7 (NPHS7), also known as phospholipase C epsilon 1 deficiency. NPHS7 is a rare genetic disorder characterized by proteinuria (excessive protein in the urine), nephrotic syndrome (a kidney disorder), and chronic kidney disease. NGS (Next-Generation Sequencing) genetic testing refers to a high-throughput DNA sequencing technology that can analyze multiple genes simultaneously. In the context of NPHS7, NGS genetic testing can be used to identify mutations or variants in the DGKE gene that may be responsible for the development of the disease. NGS genetic testing for NPHS7 can help with accurate diagnosis, genetic counseling, and management of individuals with suspected or confirmed NPHS7. It can also assist in identifying family members who may be at risk of inheriting the condition. It is important to note that NGS genetic testing for NPHS7 is typically performed by specialized laboratories and should be ordered and interpreted by healthcare professionals with expertise in genetics. Genetic counseling is also recommended to discuss the implications of the test results and the inheritance pattern of NPHS7. |
