Mitochondrial Trifunctional Protein Deficiency

Mitochondrial trifunctional protein deficiency is an autosomal recessive fatty acid oxidation disorder that prevents the body from converting certain fats to energy, particularly during periods without food . People with this disorder have inadequate levels of an enzyme that breaks down a certain group of fats called long-chain fatty acids.

Read more about Mitochondrial Trifunctional Protein Deficiency:  Signs and Symptoms, Genetics, Pathophysiology, Diagnosis, Treatment, Epidemiology

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