PRPH2 Gene Fundus albipunctatus Genetic Test
Components:
- Test Name: PRPH2 Gene Fundus albipunctatus 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: Ophthalmology Disorders
- Doctor: Ophthalmologist
- Test Department: Genetics
Pre Test Information:
Clinical History of Patient who is going for PRPH2 Gene Fundus albipunctatus NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRPH2 Gene Fundus albipunctatus NGS Genetic DNA Test gene PRPH2.
Test Details:
The PRPH2 gene is associated with Fundus albipunctatus, a rare genetic disorder that affects the retina of the eye. This condition is characterized by the presence of white or yellow spots on the retina, which can cause vision problems such as reduced visual acuity and night blindness.
NGS (Next-Generation Sequencing) genetic testing is a diagnostic tool that can identify mutations in the PRPH2 gene. This test involves sequencing the entire coding region of the gene to detect any changes or abnormalities that may be causing the disease. NGS testing can provide a definitive diagnosis of Fundus albipunctatus and can help guide treatment and management strategies. It can also be used for genetic counseling and to identify family members who may be at risk for the condition.
Overall, NGS genetic testing for the PRPH2 gene is an important tool for the diagnosis and management of Fundus albipunctatus.
Test Name | PRPH2 Gene Fundus albipunctatus 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 | Ophthalmology Disorders |
Doctor | Ophthalmologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for PRPH2 Gene Fundus albipunctatus NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRPH2 Gene Fundus albipunctatus NGS Genetic DNA Test gene PRPH2 |
Test Details | The PRPH2 gene is associated with Fundus albipunctatus, a rare genetic disorder that affects the retina of the eye. This condition is characterized by the presence of white or yellow spots on the retina, which can cause vision problems such as reduced visual acuity and night blindness. NGS (Next-Generation Sequencing) genetic testing is a diagnostic tool that can identify mutations in the PRPH2 gene. This test involves sequencing the entire coding region of the gene to detect any changes or abnormalities that may be causing the disease. NGS testing can provide a definitive diagnosis of Fundus albipunctatus and can help guide treatment and management strategies. It can also be used for genetic counseling and to identify family members who may be at risk for the condition. Overall, NGS genetic testing for the PRPH2 gene is an important tool for the diagnosis and management of Fundus albipunctatus. |