NDLI: Unsuccessful switch from insulin to sulfonylurea therapy in permanent neonatal diabetes mellitus due to an R201H mutation in the KCNJ11 gene: a case report.

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Heo, Jeong Won Kim, Sang-Wook Cho, Eun-Hee
Description	Author Affiliation: Heo JW ( Department of Internal Medicine, Kangwon National University Hospital, School of Medicine, Kangwon National University, 26 Kangwondaehak-gil, Chuncheon-si, Gangwon-do 200-701, Republic of Korea.)
Abstract	Mutations in KCNJ11 are a common cause of permanent neonatal diabetes mellitus. Previously, all patients carrying an R201H mutation in the KCNJ11 gene showed successful switches from insulin to sulfonylurea. Here, we report an unsuccessful switch in an 18-year-old patient carrying the common R201H mutation in the KCNJ11 gene.
File Format	HTM / HTML
ISSN	01688227
Issue Number	1
Volume Number	100
e-ISSN	18728227
Journal	Diabetes Research and Clinical Practice
Language	English
Publisher	Elsevier
Publisher Date	2013-04-01
Publisher Place	Ireland
Access Restriction	One Nation One Subscription (ONOS)
Subject Keyword	Administration, Oral Potassium Channels, Inwardly Rectifying Hemoglobin A, Glycosylated Humans Drug Therapy Blood Glucose Male Mutation, Missense Metabolism Insulin Therapeutic Use Blood Journal Article Case Reports Hypoglycemic Agents Glyburide Histidine Arginine Discipline Endocrinology Treatment Failure Adolescent Diabetes Mellitus, Type 1 Genetics Sulfonylurea Compounds
Content Type	Text
Resource Type	Case study Article
Subject	Endocrinology, Diabetes and Metabolism Internal Medicine Endocrinology

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Unsuccessful switch from insulin to sulfonylurea therapy in permanent neonatal diabetes mellitus due to an R201H mutation in the KCNJ11 gene: a case report.