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Stargardt disease 3

Stargardt disease 3: Introduction

Stargardt disease 3: A rare genetic eye disorder that affects children and involves degeneration of the macula which is responsible for central vision which allows detailed visual function such as reading. Type 3 is caused by a defect in the ELOVL4 gene. More detailed information about the symptoms, causes, and treatments of Stargardt disease 3 is available below.

Symptoms of Stargardt disease 3

Home Diagnostic Testing

Home medical testing related to Stargardt disease 3:

Wrongly Diagnosed with Stargardt disease 3?

Causes of Stargardt disease 3

Read more about causes of Stargardt disease 3.

Stargardt disease 3: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Stargardt disease 3: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Stargardt disease 3: Animations

Stargardt disease 3: Broader Related Topics

User Interactive Forums

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Related Stargardt disease 3 Info

More information about Stargardt disease 3

  1. Stargardt disease 3: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing

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