Ophthalmology Genetic Testing

Protect Your Vision with Personalized Insights

Early Detection and Targeted Care for Inherited Eye Disorders

Your vision health is deeply connected to your DNA, shaping how your eyes develop, function, and adapt to environmental challenges. Ophthalmology genetic testing uncovers inherited risks, providing insights into conditions like retinal dystrophies, glaucoma, and congenital cataracts. With personalized genetic insights, you can customize treatments, implement preventive strategies, and optimize care for your unique profile, empowering you to safeguard and improve your vision health.

Why Choose Ophthalmology Genetic Testing?

  • Early Detection: Identify genetic risks for eye disorders before symptoms progress.
  • Personalized Treatment Plans: Tailored solutions for vision correction, disease management, and preventive care.
  • Family Health Insights: Understand hereditary risks and help family members take preventive steps.
  • Improved Quality of Life: Manage vision health effectively and enjoy a clearer, brighter future.

Who Should Consider Ophthalmology Consultation?

  • Individuals with a family history of eye diseases like glaucoma, macular degeneration, or retinitis pigmentosa.
  • People experiencing unexplained vision loss, night blindness, or light sensitivity.
  • Those diagnosed with congenital eye conditions or early-onset vision problems.
  • Patients with a history of genetic syndromes affecting the eyes (e.g., Marfan syndrome, Stickler syndrome).
  • Anyone seeking to understand their genetic risks and take proactive steps for vision health.

Common Ophthalmology Conditions We Address

  • Achromatopsia Panel
  • Albinism Panel
  • Bardet-Biedl Syndrome Panel
  • Cataract Panel
  • Cone Rod Dystrophy Panel
  • Congenital Stationary Night Blindness Panel
  • Corneal Dystrophy Panel
  • Ectopia Lentis Panel
  • Flecked Retina Disorders Panel
  • Glaucoma Panel
  • Joubert Syndrome Panel
  • Leber Congenital Amaurosis Panel
  • Macular Dystrophy Panel
  • Microphthalmia, Anophthalmia and Anterior Segment Dysgenesis Panel
  • Neuro-Ophthalmology Panel
  • Optic Atrophy Panel
  • Retinal Dystrophy Panel
  • Retinitis Pigmentosa Panel
  • Senior-Loken Syndrome Panel
  • Septo-Optic Dysplasia Panel
  • Stickler Syndrome Panel
  • Usher Syndrome Panel
  • Vitreoretinopathy Panel

Comprehensive Genes List

A4GALT, A4GNT, AAAS, AADAC, AADACL2, AAGAB, AANAT, AARS, AARS2, AASS, ABAT, ABCA1, ABCA10, ABCA12, ABCA13, ABCA2, ABCA3, ABCA4, ABCA5, ABCA7, ABCB1, ABCB11, ABCB4, ABCB5, ABCB6, ABCB7, ABCC1, ABCC11, ABCC12, ABCC2, ABCC3, ABCC4, ABCC6, ABCC8, ABCC9, ABCD1, ABCD3, ABCD4, ABCG1, ABCG2, ABCG5, ABCG8, ABHD1, ABHD12, ABHD5, ABI3BP, ABL1, ABL2, ABO, ABRAXAS1, ACACA, ACACB, ACAD10, ACAD11, ACAD8, ACAD9, ACADL, ACADM, ACADS, ACADSB, ACADVL, ACAN, ACAT1, ACAT2, ACBD5, ACBD6, ACCS, ACE, ACHE, ACKR1, ACKR3, ACLY, ACMSD, ACO2, ACOX1, ACP1, ACP2, ACP5, ACP6,

How It Works?

  1. Consultation: Discuss your symptoms, family history, and concerns with an ophthalmology specialist.
  2. Sample Collection: Provide a simple saliva or blood sample for DNA analysis.
  3. Advanced Genetic Analysis: State-of-the-art testing detects key genetic mutations linked to vision health.
  4. Personalized Report: Receive a detailed, easy-to-understand report with actionable insights.
  5. Expert Guidance: Work with ophthalmologists and genetic counselors to create a tailored care plan.

Why Choose Us?

  • Cutting-Edge Technology: Advanced genetic sequencing for precise and reliable results.
  • Expert Team: Board-certified ophthalmologists and genetic counselors guiding you every step of the way.
  • Privacy Assurance: Your genetic data is protected with strict confidentiality policies.
  • Compassionate Care: Dedicated to your comfort, well-being, and long-term vision health.