Makale detayı · 2023
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 Endocrinologica (Bucharest)
- Yıl
- 2023
- ISSN
1841-0987- Tür
- article
Veri kaynağı ayrımı
- YÖKSİS YÖKSİS makale kaydı
- OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)
Özet
İngilizce (OpenAlex)
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.
Konular
- Neonatal Health and Biochemistry
- Erythrocyte Function and Pathophysiology
- Hyperglycemia and glycemic control in critically ill and hospitalized patients
Birincil konu Neonatal Health and Biochemistry