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.
See full list of 31 symptoms of Cytochrome c oxydase deficiency, French-Canadian type
Read more about causes of Cytochrome c oxydase deficiency, French-Canadian type.
Read more about symptoms of 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...read more »
Read more about Misdiagnosis and Cytochrome c oxydase deficiency, French-Canadian type
Types of Cytochrome c oxydase deficiency, French-Canadian type
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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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