Pyruvate carboxylase deficiency type C as a differential diagnosis of diabetic ketoacidosis.
Neslihan DoğuluÜmmühan ÖncülEngin KöseZehra AycanFatma Tuba EminoğluPublished 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.