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The congenital lactic acidosis represent a sizable group of metabolic disorders.
They are in all likelihood genetically determined, and they are clearly heterogenous. They may be
considered broadly as disorders of pyruvate metabolism in which there are two general categories:
defects in gluconeogenesis and defects in pyruvate oxidation.
We experienced a case of congenital lactic acidosis in neonate who was diagnosed by urinary
organic acid... |
