Congenital lactic acidosis is defined by the presence of a metabolic acidosis due to the accumulation of lactic acid in blood. Congenital defects of any one of the multiple enzymatic steps of pyruvate utilization induce accumulation of pyruvate and l

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fatale infantiele lactaatacidose gelijktijdig met methylmalonacidurie

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A rare inborn error of metabolism disorder with early-onset acute encephalopathic episodes (frequently triggered by viral infections) associated with lactic acidosis and alpha-ketoglutaric aciduria which typically manifest with variable degrees of at

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encefalopathie in kinderjaren door thiaminepyrofosfokinasedeficiëntie

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respiratory acidosis

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respiratore acidose

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decompensated acidosis

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ongecompenseerde acidose

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Lightwood-Albright syndrome Renal tubular acidosis NOS Secondary hyperparathyroidism of renal origin

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renale tubulusacidose NNO | secundaire hyperparathyroïdie van renale oorsprong | syndroom van Lightwood-Albright

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IN-CONTEXT TRANSLATIONS

The following rows are inserted between the row of the particular nutritional purpose ‘Reduction of the risk of acidosis’ and the row for the particular nutritional purpose ‘Stabilisation of water and electrolyte balance’:

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De volgende rijen worden ingevoegd tussen de rij van bijzonder voedingsdoel „Vermindering van het risico van acidose” en de rij van bijzonder voedingsdoel „Stabilisatie van de water- en elektrolytenbalans”:

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Anderen hebben gezocht naar : acidosis acidosis nos diabetic acidosis decompensated acidosis high blood acidity lactic metabolic respiratory respiratory acidosis

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Date index: 2022-11-14