Clinical, Genetic Features and Treatment Results in Patients with Congenital Hyperinsulinemic Hypoglycemia: A Single Center Experience
GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS, vol.18, no.3, pp.317-335, 2020 (ESCI, Scopus)
- Publication Type: Article / Article
- Volume: 18 Issue: 3
- Publication Date: 2020
- Journal Name: GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS
- Journal Indexes: Emerging Sources Citation Index (ESCI), Scopus, Academic Search Premier, CAB Abstracts, CINAHL, EMBASE, Veterinary Science Database
- Page Numbers: pp.317-335
- Keywords: diazoxide, hyperinsulinism, hypoglycaemia, neuroglycopenic symptom, KATP channel, 11P15 IMPRINTED GENES, TERM-FOLLOW-UP, LONG-TERM, SURGICAL-MANAGEMENT, TURKISH PATIENTS, MUTATIONS, CHILDREN, ABCC8, DIAGNOSIS, INFANCY
- Dokuz Eylül University Affiliated: Yes
Abstract
INTRODUCTION: Congenital hyperinsulinemic hypoglycemia is a rare disease caused by uncontrolled release of insulin from the pancreas. In this study, we aimed to evaluate the clinical and genetic characteristics and prognosis of the patients with congenital hyperinsulinemic hypoglycemia.