A successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up.

2.50
Hdl Handle:
http://hdl.handle.net/11287/620375
Title:
A successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up.
Authors:
Katanic, D.; Vorgučin, I.; Hattersley, Andrew T.; Ellard, Sian ( 0000-0002-7620-5526 ) ; Houghton, Jayne A. L.; Obreht, D.; Knežević Pogančev, M.; Vlaški, J.; Pavkov, D.
Abstract:
Neonatal diabetes mellitus is a rare monogenic disease with incidence of 1/90,000 newborns. A case of two months aged male infant with life threatening diabetic ketoacidosis is presented with novel ABCC8 gene mutation (p.F577L), successful transition from insulin to sulfonylurea and follow-up of three years.
Citation:
A successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up. 2017, 129:59-61 Diabetes Res. Clin. Pract.
Publisher:
Elsevier
Journal:
Diabetes research and clinical practice
Issue Date:
Jul-2017
URI:
http://hdl.handle.net/11287/620375
DOI:
10.1016/j.diabres.2017.04.021
PubMed ID:
28511139
Additional Links:
https://linkinghub.elsevier.com/retrieve/pii/S0168-8227(16)30581-2
Type:
Journal Article
Language:
en
ISSN:
1872-8227
Appears in Collections:
2017 RD&E publications

Full metadata record

DC FieldValue Language
dc.contributor.authorKatanic, D.en
dc.contributor.authorVorgučin, I.en
dc.contributor.authorHattersley, Andrew T.en
dc.contributor.authorEllard, Sianen
dc.contributor.authorHoughton, Jayne A. L.en
dc.contributor.authorObreht, D.en
dc.contributor.authorKnežević Pogančev, M.en
dc.contributor.authorVlaški, J.en
dc.contributor.authorPavkov, D.en
dc.date.accessioned2017-07-20T14:15:19Z-
dc.date.available2017-07-20T14:15:19Z-
dc.date.issued2017-07-
dc.identifier.citationA successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up. 2017, 129:59-61 Diabetes Res. Clin. Pract.en
dc.identifier.issn1872-8227-
dc.identifier.pmid28511139-
dc.identifier.doi10.1016/j.diabres.2017.04.021-
dc.identifier.urihttp://hdl.handle.net/11287/620375-
dc.description.abstractNeonatal diabetes mellitus is a rare monogenic disease with incidence of 1/90,000 newborns. A case of two months aged male infant with life threatening diabetic ketoacidosis is presented with novel ABCC8 gene mutation (p.F577L), successful transition from insulin to sulfonylurea and follow-up of three years.en
dc.language.isoenen
dc.publisherElsevieren
dc.relation.urlhttps://linkinghub.elsevier.com/retrieve/pii/S0168-8227(16)30581-2en
dc.rightsArchived with thanks to Diabetes research and clinical practiceen
dc.subjectWessex Classification Subject Headings::Oncology. Pathology.::Geneticsen
dc.subjectWessex Classification Subject Headings::Endocrinology::Diabetesen
dc.titleA successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up.en
dc.typeJournal Articleen
dc.identifier.journalDiabetes research and clinical practiceen
dc.type.versionPublisheden

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