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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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Dades bibliogràfiques
Publicat a:Curr Opin Pediatr
Autors principals: Vajravelu, Mary Ellen, De León, Diva D.
Format: Artigo
Idioma:Inglês
Publicat: 2018
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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