Diagnosis and treatment of neonatal diabetes: an United States experience

Background/objective: Mutations in KCNJ11, ABCC8, or INS are the cause of permanent neonatal diabetes mellitus in about 50% of patients diagnosed with diabetes before 6 months of age and in a small fraction of those diagnosed between 6 and 12 months. The aim of this study was to identify the geneti...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Pediatric diabetes 2008-10, Vol.9 (5), p.450-459
Hauptverfasser:	Støy, Julie, Greeley, Siri Atma W, Paz, Veronica P, Ye, Honggang, Pastore, Ashley N, Skowron, Kinga B, Lipton, Rebecca B, Cogen, Fran R, Bell, Graeme I, Philipson, Louis H
Format:	Artikel
Sprache:	eng
Schlagworte:	ABCC8 Adolescent Adult ATP-Binding Cassette Transporters - genetics ATP-sensitive potassium channel Child Child, Preschool Diabetes Complications Diabetes Mellitus, Type 1 - drug therapy Diabetes Mellitus, Type 1 - genetics Female glyburide Glyburide - therapeutic use Humans Infant Infant, Newborn Insulin - genetics Insulin - therapeutic use insulin gene KCNJ11 Learning Disorders - etiology Male monogenic diabetes Pedigree Potassium Channels, Inwardly Rectifying - genetics Receptors, Drug - genetics Sulfonylurea Receptors United States - epidemiology
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!