The Diagnosis of Neonatal Diabetes in a Mother at 25 Years of Age
Author(s) -
Divya S. Khurana,
M C Contreras,
Neha Malhotra,
Renee Bargman
Publication year - 2012
Publication title -
diabetes care
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.636
H-Index - 363
eISSN - 1935-5548
pISSN - 0149-5992
DOI - 10.2337/dc11-2439
Subject(s) - medicine , glycemic , diabetes mellitus , diabetic ketoacidosis , pediatrics , ketoacidosis , endocrinology , insulin , girl , kir6.2 , gestation , type 1 diabetes , pregnancy , protein subunit , psychology , developmental psychology , biochemistry , chemistry , genetics , biology , gene
Neonatal diabetes (ND) is defined as persistent hyperglycemia in the first 3 months of life (1). Heterozygous—usually autosomal-dominant—activating mutations in KCNJ11 , which encode the Kir6.2 subunit of the ATP-potassium (KATP) channel, cause the majority of cases (2). Sulfonylureas close the KATP channel by an ATP independent route (2).A 25-year-old Bangladeshi woman with type 1 diabetes gave birth to a baby girl. The mother had been on insulin for more than 20 years with inadequate glycemic control but never ketoacidosis. The baby was small for gestational age (2.4 kg, <3%). On day 2 of her life, the baby was noted to be increasingly hyperglycemic, reaching 312 mg/dL by day 7. Given the clinical suspicion for ND, a trial of glyburide was initiated at 0.45 mg/kg/day, and the baby responded well. The …
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