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Romanian Academy
The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
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Acta Endocrinologica (Buc)
Goren TA, Kilimci DD, Yigit Y, Yildirim AT, Gulen H, Ersoy B
Episode of Acute Hemolysis Due to Undiagnosed Glucose-6-Phosphate Dehidrogenase Deficiency in an Adolescent with Newly Diagnosed Type 1 Diabetes Mellitus: Case Report and Review of Literature
Acta Endo (Buc) 2023, 19 (2): 256-259doi: 10.4183/aeb.2023.256
Glucose-6-phosphate dehydrogenase (G6PD)
enzyme deficiency is common in the community. The most
important clinical manifestation of G6PD deficiency is
acute hemolytic anemia due to oxidative stressors. Diabetes
Mellitus (DM) can precipitate hemolysis in patients with
G6PD deficiency. Here, we described a 15-year-old male
with newly diagnosed type 1 DM (T1DM) and unknown
G6PD deficiency who suffered from hemolytic anemia
during normalization of blood glucose. On admission, the
patient did not have ketoacidosis. After the patient's blood
sugars were regulated with insulin therapy, he presented
five days later with hemolytic anemia. The cause of
hemolytic anemia was G6PD deficiency. The patient had
no previous episodes of hemolysis and had no relevant
family history. Hypoglycemia did not occur during blood
glucose regulation. The return of blood sugar to normal
after a long period of hyperglycemia was thought to be
the possible cause of hemolysis. In conclusion, G6PD
deficiency should be considered when there is an episode
of hemolysis in newly diagnosed children and adolescents
with T1DM, especially in the absence of ketoacidosis and
hypoglycemia.
Keywords: Type 1 Diabetes mellitus, glucose 6 phosphate dehydrogenase deficiency, hemolysis, hemolytic anemia, hyperglycemia.
Correspondence: Tugba Aysun Gören MD, “Celal Bayar” University, Faculty of Medicine, Department of Pediatrics, Uncubozköy, Manisa, 45040, Turkey, E-mail: draysunzararsiz@gmail.com