Both Low Blood Glucose and Insufficient Treatment Confer Risk of Neurodevelopmental Impairment in Congenital Hyperinsulinism: A Multinational Cohort Study

BACKGROUND/AIMS: Congenital hyperinsulinism (CHI) is a heterogeneous disease most frequently caused by KATP-channel (ABCC8 and KCNJ11) mutations, with neonatal or later onset, variable severity, and with focal or diffuse pancreatic involvement as the two major histological types. CHI confers a high...

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Detalles Bibliográficos
Autores principales: Helleskov, Annett, Melikyan, Maria, Globa, Evgenia, Shcherderkina, Inna, Poertner, Fani, Larsen, Anna-Maria, Filipsen, Karen, Brusgaard, Klaus, Christiansen, Charlotte Dahl, Hansen, Lars Kjaersgaard, Christesen, Henrik T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502348/
https://www.ncbi.nlm.nih.gov/pubmed/28740482
http://dx.doi.org/10.3389/fendo.2017.00156

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502348/
https://www.ncbi.nlm.nih.gov/pubmed/28740482
http://dx.doi.org/10.3389/fendo.2017.00156

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