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RDH5 Gene Fundus albipunctatus Genetic Test Cost

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

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The RDH5 Gene Fundus Albipunctatus Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the RDH5 gene, which are known to cause Fundus Albipunctatus, a rare genetic disorder. This condition is characterized by an abundance of white dots in the retina, leading to night blindness or delayed dark adaptation, though vision can improve in bright light conditions. The RDH5 gene plays a crucial role in the visual cycle, and mutations can disrupt this process, leading to the symptoms observed in affected individuals.

The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in a laboratory to detect any genetic anomalies associated with the condition. It is particularly valuable for individuals showing symptoms of Fundus Albipunctatus or those with a family history of the disorder, providing crucial information for diagnosis, management, and genetic counseling.

Conducted at DNA Labs UAE, a leading facility known for its advanced genetic testing services, the RDH5 Gene Fundus Albipunctatus Genetic Test is priced at 4400 AED. The test is performed under strict quality controls and is interpreted by genetic experts, ensuring accurate and reliable results. This test not only aids in confirming the diagnosis but also helps in understanding the inheritance pattern, which is vital for affected families considering future pregnancies.

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RDH5 Gene Fundus albipunctatus Genetic Test

Components: RDH5 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 RDH5 Gene Fundus albipunctatus NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RDH5 Gene Fundus albipunctatus NGS Genetic DNA Test gene RDH5

Test Details

Fundus albipunctatus is a rare genetic eye disorder characterized by the presence of white or yellow dots in the retina. It is caused by mutations in the RDH5 gene, which encodes for an enzyme involved in the visual cycle.

NGS genetic testing for RDH5 gene mutations can help diagnose Fundus albipunctatus. This test involves sequencing the entire RDH5 gene to identify any mutations that may be present. If a mutation is found, it can confirm a diagnosis of Fundus albipunctatus and inform treatment and management options.

NGS genetic testing is a highly sensitive and specific method of genetic testing that can detect mutations in genes that are associated with inherited diseases. It is a valuable tool for identifying genetic causes of diseases and can provide important information for patients and their families.

Test Name RDH5 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 RDH5 Gene Fundus albipunctatus NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RDH5 Gene Fundus albipunctatus NGS Genetic DNA Test gene RDH5
Test Details

Fundus albipunctatus is a rare genetic eye disorder characterized by the presence of white or yellow dots in the retina. It is caused by mutations in the RDH5 gene, which encodes for an enzyme involved in the visual cycle.

NGS genetic testing for RDH5 gene mutations can help diagnose Fundus albipunctatus. This test involves sequencing the entire RDH5 gene to identify any mutations that may be present. If a mutation is found, it can confirm a diagnosis of Fundus albipunctatus and inform treatment and management options.

NGS genetic testing is a highly sensitive and specific method of genetic testing that can detect mutations in genes that are associated with inherited diseases. It is a valuable tool for identifying genetic causes of diseases and can provide important information for patients and their families.

SKU: TEST-994 Category:

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