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

Ayla Güven | Zendy; Ayşe Nurcan Cebeci | Zendy; Sian Ellard | Zendy; Sarah E. Flanagan | Zendy

Open Access

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

Author(s) -

Ayla Güven,

Ayşe Nurcan Cebeci,

Sian Ellard,

Sarah E. Flanagan

Publication year - 2016

Publication title -

journal of clinical research in pediatric endocrinology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.566

H-Index - 35

eISSN - 1308-5735

pISSN - 1308-5727

DOI - 10.4274/jcrpe.2408

Subject(s) - medicine , congenital hyperinsulinism , pancreatectomy , pediatrics , nesidioblastosis , hypoglycemia , diabetes mellitus , hyperinsulinism , genetic testing , gene mutation , gastroenterology , cohort , mutation , pancreas , insulin , endocrinology , genetics , insulin resistance , biology , gene

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.

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