Mitochondrial trifunctional protein deficiency: A rare genetic condition where the body is unable to convert certain fats to energy. More specifically, there is insufficient levels of a particular enzyme needed to metabolize a type of fat called long-chain fatty acids. More detailed information about the symptoms, causes, and treatments of Mitochondrial trifunctional protein deficiency is available below.
See full list of 9 symptoms of Mitochondrial trifunctional protein deficiency
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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 Mitochondrial trifunctional protein deficiency as a "rare disease".
Source - Orphanet
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