PDE6H Gene Achromatopsia Type 6 Genetic Test
Test Name: PDE6H Gene Achromatopsia Type 6 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
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 PDE6H Gene Achromatopsia Type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PDE6H Gene Achromatopsia Type 6 NGS Genetic DNA Test gene PDE6H
Test Details: The PDE6H gene is associated with a type of inherited retinal disorder called achromatopsia type 6. This condition is characterized by a lack of color vision, reduced visual acuity, sensitivity to bright light, and nystagmus (involuntary eye movements). NGS genetic testing for PDE6H mutations can identify individuals who are at risk of developing achromatopsia type 6 or who already have the condition. This information can be used to inform medical management and genetic counseling for affected individuals and their families. NGS genetic testing involves sequencing the DNA of an individual to identify any mutations or variations in the PDE6H gene. This type of testing is highly accurate and can identify even rare mutations that may be missed by other genetic testing methods. Overall, NGS genetic testing for PDE6H mutations can provide important information for the diagnosis, management, and genetic counseling of individuals with achromatopsia type 6.
| Test Name | PDE6H Gene Achromatopsia type 6 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 PDE6H Gene Achromatopsia type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PDE6H Gene Achromatopsia type 6 NGS Genetic DNA Test gene PDE6H |
| Test Details | The PDE6H gene is associated with a type of inherited retinal disorder called achromatopsia type 6. This condition is characterized by a lack of color vision, reduced visual acuity, sensitivity to bright light, and nystagmus (involuntary eye movements). NGS genetic testing for PDE6H mutations can identify individuals who are at risk of developing achromatopsia type 6 or who already have the condition. This information can be used to inform medical management and genetic counseling for affected individuals and their families. NGS genetic testing involves sequencing the DNA of an individual to identify any mutations or variations in the PDE6H gene. This type of testing is highly accurate and can identify even rare mutations that may be missed by other genetic testing methods. Overall, NGS genetic testing for PDE6H mutations can provide important information for the diagnosis, management, and genetic counseling of individuals with achromatopsia type 6. |
