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Pyruvate carboxylase deficiency type C as a differential diagnosis of diabetic ketoacidosis.

Neslihan DoğuluÜmmühan ÖncülEngin KöseZehra AycanFatma Tuba Eminoğlu
Published in: Journal of pediatric endocrinology & metabolism : JPEM (2021)
To date, there have been no reports in literature of type C phenotype patients manifesting with DKA. Our case is the first case with the type C phenotype to be admitted with clinical and laboratory findings of DKA.
Keyphrases
  • end stage renal disease
  • chronic kidney disease
  • ejection fraction
  • systematic review
  • newly diagnosed
  • type diabetes
  • peritoneal dialysis
  • prognostic factors
  • patient reported outcomes
  • smoking cessation