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SUN-272 Persistent Hyperinsulinemic Hypoglycemia Due to Mutation in Hepatocyte Nuclear Factor 4A
Background: Congenital hyperinsulinism (HI) is the most common cause of hypoglycemia in children. Delay in diagnosis and or inadequate management can lead to brain damage. Persistent hyperinsulinemic hypoglycemia of infancy is a genetic disorder with both familial and sporadic form. Aim: To present...
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| Publicado no: | J Endocr Soc |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Endocrine Society
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6552805/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SUN-272 |
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