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Up to: Mitochondrial oxidative phosphorylation disorder · Acute liver failure · Infantile liver failure
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Acute infantile liver failure due to mtDNA-encoded proteins synthesis defect is a very rare mitochondrial respiratory chain deficiency described in fewer than 10 infants, primarily of middle Eastern descent, and characterized clinically by transient but life-threatening liver failure with elevated liver enzymes, jaundice, vomiting, coagulopathy, hyperbilirubinemia, and lactic acidemia.
This condition has no sub-types.