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PDE6H Gene Achromatopsia Type 6 Genetic Test

Name: PDE6H Gene Achromatopsia Type 6 Genetic Test
SKU: TEST-905
Price: 4400 AED
Availability: InStock

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The PDE6H gene achromatopsia type 6 genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the PDE6H gene, which are linked to achromatopsia type 6. Achromatopsia is a rare, inherited eye condition characterized by partial or total absence of color vision, light sensitivity, and reduced visual acuity. The test plays a crucial role in the accurate diagnosis and understanding of this specific type of achromatopsia, enabling tailored patient care and management strategies.

DNA Labs UAE, known for its advanced genetic testing services, performs this test with precision and reliability. The cost of the test is set at 4400 AED, reflecting the intricate processes and sophisticated technology involved in detecting the genetic variations associated with the condition. Through this test, individuals and families gain valuable insights into their genetic makeup, paving the way for informed decisions regarding treatment options and lifestyle adjustments to better manage the condition.

Description

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.