The University of Southampton
University of Southampton Institutional Repository

6q24 transient neonatal diabetes

6q24 transient neonatal diabetes
6q24 transient neonatal diabetes
Transient Neonatal Diabetes (type 1) is the commonest cause of diabetes presenting in the first week of life. The majority of infants recover by 3 months of age but are predisposed to developing type 2 diabetes in later life. It is associated with low birth weight but rapid catch up by 1 year of life. The condition is usually due to genetic or epigenetic aberrations at an imprinted locus on chromosome 6q24 and can be sporadic or inherited. Early diagnosis alters medical treatment strategies and differentiates it from other types of early onset diabetes. In some individuals, diabetes may be the initial presentation of a more complex imprinting disorder due to recessive mutations in the gene ZFP57 and may be associated with other developmental problems
1389-9155
199-204
Temple, I. Karen
d63e7c66-9fb0-46c8-855d-ee2607e6c226
Shield, Julian P.H.
b7c65f5e-9a39-429d-8c1a-8ffd911abe71
Temple, I. Karen
d63e7c66-9fb0-46c8-855d-ee2607e6c226
Shield, Julian P.H.
b7c65f5e-9a39-429d-8c1a-8ffd911abe71

Temple, I. Karen and Shield, Julian P.H. (2010) 6q24 transient neonatal diabetes. Reviews in Endocrine & Metabolic Disorders, 11 (3), 199-204. (doi:10.1007/s11154-010-9150-4). (PMID:20922569)

Record type: Article

Abstract

Transient Neonatal Diabetes (type 1) is the commonest cause of diabetes presenting in the first week of life. The majority of infants recover by 3 months of age but are predisposed to developing type 2 diabetes in later life. It is associated with low birth weight but rapid catch up by 1 year of life. The condition is usually due to genetic or epigenetic aberrations at an imprinted locus on chromosome 6q24 and can be sporadic or inherited. Early diagnosis alters medical treatment strategies and differentiates it from other types of early onset diabetes. In some individuals, diabetes may be the initial presentation of a more complex imprinting disorder due to recessive mutations in the gene ZFP57 and may be associated with other developmental problems

This record has no associated files available for download.

More information

Published date: September 2010

Identifiers

Local EPrints ID: 166445
URI: http://eprints.soton.ac.uk/id/eprint/166445
ISSN: 1389-9155
PURE UUID: 00111a22-c4cb-46ee-a5b3-f57e89136d8c
ORCID for I. Karen Temple: ORCID iD orcid.org/0000-0002-6045-1781

Catalogue record

Date deposited: 28 Oct 2010 13:57
Last modified: 14 Mar 2024 02:42

Export record

Altmetrics

Contributors

Author: I. Karen Temple ORCID iD
Author: Julian P.H. Shield

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×