Persistent neonatal hypoglycemia secondary to hyperinsulinism/hyperammonemia. Case report
Introduction: Hyperinsulinism/hyperammonemia syndrome (HI/HA) is a rare genetic disease caused by the activation of mutations in the GLUD1 gene. It is characterized by recurrent symptomatic hypoglycemic episodes, poor tolerance to fasting, and requirement for high metabolic fluxes of glucose, with a...
I tiakina i:
| Ngā kaituhi matua: | , , |
|---|---|
| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
Universidad Nacional de Colombia
2022-10-01
|
| Rangatū: | Revista de la Facultad de Medicina |
| Ngā marau: | |
| Urunga tuihono: | https://revistas.unal.edu.co/index.php/revfacmed/article/view/93016 |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
|