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Progressive External Opthhalmoplegia, Autosomal Dominant, 1

Progressive External Opthhalmoplegia, Autosomal Dominant, 1: Introduction

Progressive External Opthhalmoplegia, Autosomal Dominant, 1: A slow progressive paralysis of the motor nerves of the eye (external eye muscles). The condition is often abbreviated to PEO and is caused by a mitochondrial disease called mitochondrial myopathy which affects the muscles which can include the eye muscles. There are a number of different subtypes, each linked to a different genetic defect. Type 1 is linked to a defect on chromosome 15q25. More detailed information about the symptoms, causes, and treatments of Progressive External Opthhalmoplegia, Autosomal Dominant, 1 is available below.

Symptoms of Progressive External Opthhalmoplegia, Autosomal Dominant, 1

Home Diagnostic Testing

Home medical testing related to Progressive External Opthhalmoplegia, Autosomal Dominant, 1:

Wrongly Diagnosed with Progressive External Opthhalmoplegia, Autosomal Dominant, 1?

Causes of Progressive External Opthhalmoplegia, Autosomal Dominant, 1

  • A genetic defect on chromosome 15q25 inherited in an autosomal dominant manner
  • more causes...»

More information about causes of Progressive External Opthhalmoplegia, Autosomal Dominant, 1:

Less Common Symptoms of Progressive External Opthhalmoplegia, Autosomal Dominant, 1

Progressive External Opthhalmoplegia, Autosomal Dominant, 1: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Progressive External Opthhalmoplegia, Autosomal Dominant, 1

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Progressive External Opthhalmoplegia, Autosomal Dominant, 1: Research Doctors & Specialists

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Progressive External Opthhalmoplegia, Autosomal Dominant, 1: Animations

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More information about Progressive External Opthhalmoplegia, Autosomal Dominant, 1

  1. Progressive External Opthhalmoplegia, Autosomal Dominant, 1: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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