Clinical and genetic characteristics, management and long-term follow-Up of Turkish Patients with Congenital Hyperinsulinism.
Date
2016-06-05Journal
Journal of clinical research in pediatric endocrinologyType
Journal ArticlePublisher
GalenosDOI
10.4274/jcrpe.2408Rights
Archived with thanks to Journal of clinical research in pediatric endocrinologyMetadata
Show full item recordAbstract
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.