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...
Sábháilte in:
| Príomhchruthaitheoirí: | , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe / Cruthaithe: |
Universidad Nacional de Colombia
2022-10-01
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| Sraith: | Revista de la Facultad de Medicina |
| Ábhair: | |
| Rochtain ar líne: | https://revistas.unal.edu.co/index.php/revfacmed/article/view/93016 |
| Clibeanna: |
Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!
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