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Congenital Hyperinsulinism Disorders: Genetic and Clinical Characteristics
Congenital hyperinsulinism (HI) is the most frequent cause of persistent hypoglycemia in infants and children. Delays in diagnosis and initiation of appropriate treatment contribute to a high risk of neurocognitive impairment. HI represents a heterogeneous group of disorders characterized by dysregu...
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| Publicat a: | Am J Med Genet C Semin Med Genet |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7229866/ https://ncbi.nlm.nih.gov/pubmed/31414570 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.c.31737 |
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