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Cytochrome c oxydase deficiency, French-Canadian type

Cytochrome c oxydase deficiency, French-Canadian type: Introduction

Cytochrome c oxydase deficiency, 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 Cytochrome c oxydase deficiency, French-Canadian type is available below.

Symptoms of Cytochrome c oxydase deficiency, French-Canadian type

Wrongly Diagnosed with Cytochrome c oxydase deficiency, French-Canadian type?

Causes of Cytochrome c oxydase deficiency, French-Canadian type

Read more about causes of Cytochrome c oxydase deficiency, French-Canadian type.

Less Common Symptoms of Cytochrome c oxydase deficiency, French-Canadian type

Misdiagnosis and Cytochrome c oxydase deficiency, French-Canadian type

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See symptoms of Vitamin B12...read more »

Statistics for Cytochrome c oxydase deficiency, French-Canadian type

Cytochrome c oxydase deficiency, French-Canadian type: Broader Related Topics

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Definitions of Cytochrome c oxydase deficiency, French-Canadian type:

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

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More information about Cytochrome c oxydase deficiency, French-Canadian type

  1. Cytochrome c oxydase deficiency, French-Canadian type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
 

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