Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism

OBJECTIVE: Mutations in the KATP channel genes is the most common cause of congenital hyperinsulinism (CHI) of infancy. Our aim was to report the clinical and genetic characteristics, treatment modalities, and long-term prognosis of patients with CHI. METHODS: Clinical and biochemical findings, oper...

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Detalles Bibliográficos
Autores principales: Güven, Ayla, Cebeci, Ayşe Nurcan, Ellard, Sian, Flanagan, Sarah E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096476/
https://www.ncbi.nlm.nih.gov/pubmed/26758964
http://dx.doi.org/10.4274/jcrpe.2408

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096476/
https://www.ncbi.nlm.nih.gov/pubmed/26758964
http://dx.doi.org/10.4274/jcrpe.2408

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