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RLBP1 Gene Bothnia Retinal Dystrophy Genetic Test

4,400 د.إ

-21%

The RLBP1 Gene Bothnia Retinal Dystrophy Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the RLBP1 gene, which are associated with Bothnia Retinal Dystrophy. This genetic condition is a form of retinal dystrophy that predominantly affects vision, leading to symptoms such as night blindness and progressive loss of visual fields. Early and accurate diagnosis through genetic testing is crucial for the management and understanding of the condition, allowing affected individuals and their families to make informed decisions regarding treatment and lifestyle adjustments.

The test is priced at 4400 AED and involves collecting a DNA sample from the patient, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific genetic mutations in the RLBP1 gene. DNA Labs UAE, where this test is conducted, is equipped with state-of-the-art technology and staffed by experienced professionals to ensure accurate and reliable results.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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RLBP1 Gene Bothnia retinal dystrophy Genetic Test

Components: RLBP1 Gene Bothnia retinal dystrophy 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 RLBP1 Gene Bothnia retinal dystrophy NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RLBP1 Gene Bothnia retinal dystrophy NGS Genetic DNA Test gene RLBP1

Test Details

The RLBP1 gene is associated with Bothnia retinal dystrophy, a rare inherited eye disorder that affects the retina, the light-sensitive tissue at the back of the eye. Mutations in the RLBP1 gene can cause a buildup of toxic byproducts in the retina, leading to progressive vision loss.

NGS (next-generation sequencing) genetic testing can identify mutations in the RLBP1 gene that may be responsible for Bothnia retinal dystrophy. This type of testing uses advanced sequencing technology to analyze multiple genes simultaneously, providing a more comprehensive and accurate diagnosis than traditional genetic testing methods.

NGS genetic testing for Bothnia retinal dystrophy may be recommended for individuals with a family history of the condition or those who are experiencing symptoms such as night blindness, decreased visual acuity, and visual field loss. Early diagnosis and genetic counseling can help individuals and families understand the inheritance pattern of the condition and make informed decisions about family planning and management of the disease.

Test Name RLBP1 Gene Bothnia retinal dystrophy 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 RLBP1 Gene Bothnia retinal dystrophy NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RLBP1 Gene Bothnia retinal dystrophy NGS Genetic DNA Test gene RLBP1
Test Details

The RLBP1 gene is associated with Bothnia retinal dystrophy, a rare inherited eye disorder that affects the retina, the light-sensitive tissue at the back of the eye. Mutations in the RLBP1 gene can cause a buildup of toxic byproducts in the retina, leading to progressive vision loss.

NGS (next-generation sequencing) genetic testing can identify mutations in the RLBP1 gene that may be responsible for Bothnia retinal dystrophy. This type of testing uses advanced sequencing technology to analyze multiple genes simultaneously, providing a more comprehensive and accurate diagnosis than traditional genetic testing methods.

NGS genetic testing for Bothnia retinal dystrophy may be recommended for individuals with a family history of the condition or those who are experiencing symptoms such as night blindness, decreased visual acuity, and visual field loss. Early diagnosis and genetic counseling can help individuals and families understand the inheritance pattern of the condition and make informed decisions about family planning and management of the disease.