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Leigh syndrome, French Canadian type

Leigh syndrome, French Canadian type: Introduction

Leigh syndrome, French Canadian type: A rare, progressive, inherited metabolic disorder where a deficiency of the enzyme cytochrome C oxidase affects skeletal muscles, connective tissue, brain and liver. More detailed information about the symptoms, causes, and treatments of Leigh syndrome, French Canadian type is available below.

Symptoms of Leigh syndrome, French Canadian type

Home Diagnostic Testing

Home medical testing related to Leigh syndrome, French Canadian type:

Wrongly Diagnosed with Leigh syndrome, French Canadian type?

Leigh syndrome, French Canadian type: Related Patient Stories

Leigh syndrome, French Canadian type: Deaths

Read more about Deaths and Leigh syndrome, French Canadian type.

Causes of Leigh syndrome, French Canadian type

Read more about causes of Leigh syndrome, French Canadian type.

Disease Topics Related To Leigh syndrome, French Canadian type

Research the causes of these diseases that are similar to, or related to, Leigh syndrome, French Canadian type:

Less Common Symptoms of Leigh syndrome, French Canadian type

Leigh syndrome, French Canadian type: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Leigh syndrome, French Canadian type

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Leigh syndrome, French Canadian type: Research Doctors & Specialists

Research related physicians and medical specialists:

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Leigh syndrome, French Canadian type: Animations

Statistics for Leigh syndrome, French Canadian type

Leigh syndrome, French Canadian type: Broader Related Topics

User Interactive Forums

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Definitions of Leigh syndrome, French Canadian type:

Leigh syndrome, French Canadian type is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Leigh syndrome, French Canadian type, or a subtype of Leigh syndrome, French Canadian type, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Leigh syndrome, French Canadian type as a "rare disease".
Source - Orphanet

 

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