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Genetic Characteristics of Patients with Congenital Hyperinsulinism
PURPOSE OF REVIEW: Congenital hyperinsulinism (HI) is the most common cause of persistent hypoglycemia in infants and children. Early and appropriate recognition and treatment of hypoglycemia is vital to minimize neurocognitive impairment. RECENT FINDINGS: There are at least 11 known monogenic forms...
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| Publicat a: | Curr Opin Pediatr |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6084463/ https://ncbi.nlm.nih.gov/pubmed/29750770 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MOP.0000000000000645 |
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