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Pasireotide treatment for severe congenital hyperinsulinism due to a homozygous ABCC8 mutation

ABCC8 and KCJN11 mutations cause the most severe diazoxide-resistant forms of congenital hyperinsulinism (CHI). Somatostatin analogues are considered as secondline treatment in diazoxide-unresponsive cases. Current treatment protocols include the first-generation somatostatin analogue octreotide, al...

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Detalles Bibliográficos
Autores principales:	Mooij, Christiaan F., Tacke, Carline E., van Albada, Mirjam E., Barthlen, Winfried, Bikker, Hennie, Mohnike, Klaus, Oomen, Matthijs W.N., van Trotsenburg, A.S. Paul, Zwaveling-Soonawala, Nitash
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Society of Pediatric Endocrinology 2021
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8749021/ https://www.ncbi.nlm.nih.gov/pubmed/33971706 http://dx.doi.org/10.6065/apem.2142010.005

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