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Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins

rare

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.

Causal genes
TRMU
Also known as
acute infantile liver failure due to synthesis defect of mitochondrial DNA-encoded proteins · infantile liver failure caused by mutation in TRMU · LFIT · liver failure, infantile, transient · liver failure, transient infantile

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