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Case report: Congenital hyperinsulinemia with ABCC8 gene mutations

BACKGROUND: Congenital hyperinsulinemia (CHI) is an inherited disease of abnormal insulin secretion and is the main cause of persistent and intractable hypoglycemia in infants. The aim of this case report was to investigate the genetic mechanisms and treatment of CHI in an affected patient. CASE SUM...

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Detalles Bibliográficos
Autores principales:	Zhang, Jin, Wang, Jiyang, Chen, Hui
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403267/ https://www.ncbi.nlm.nih.gov/pubmed/36034573 http://dx.doi.org/10.3389/fped.2022.914267

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