Clinical and genetic characteristics, management and long-term follow-Up of Turkish Patients with Congenital Hyperinsulinism.
Cebeci, A. N.
JournalJournal of clinical research in pediatric endocrinology
RightsArchived with thanks to Journal of clinical research in pediatric endocrinology
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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.