UCL  IRIS
Institutional Research Information Service
UCL Logo
Please report any queries concerning the funding data grouped in the sections named "Externally Awarded" or "Internally Disbursed" (shown on the profile page) to your Research Finance Administrator. Your can find your Research Finance Administrator at https://www.ucl.ac.uk/finance/research/rs-contacts.php by entering your department
Please report any queries concerning the student data shown on the profile page to:

Email: portico-services@ucl.ac.uk

Help Desk: http://www.ucl.ac.uk/ras/portico/helpdesk
Publication Detail
Genetics and pathophysiology of hyperinsulinism in infancy
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Article
  • Authors:
    Cosgrove KE, Shepherd RM, Fernandez EM, Natarajan A, Lindley KJ, Aynsley-Green A, Dunne MJ
  • Publication date:
    2004
  • Pagination:
    270, 288
  • Journal:
    Hormone Research
  • Volume:
    61
  • Issue:
    6
  • Print ISSN:
    0301-0163
  • Keywords:
    A, AND, ARTICLE, BETA-CELL, Channel, CHANNELS, CHILDHOOD, Condition, DEFECT, DEFECTS, DISEASE, DISORDER, DYSFUNCTION, enzyme, Enzymes, FOR, FUNCTION, GENE, Genes, Genetic, genetics, Glucokinase, HISTOPATHOLOGY, hyperinsulinism, IM, INFANCY, IS, JOURNAL, Knowledge, LA, LEVEL, METABOLISM, MOLECULAR, MUTATION, MUTATIONS, NEONATE, neonates, OF, pathophysiology, PHYSIOLOGY, relationship, Result, REVIEW, THE, UK, Unknown
  • Addresses:
    School of Biological Sciences, Stopford Building, University of Manchester, Manchester, UK
  • Notes:
    DA - 20040607 IS - 0301-0163 LA - eng PT - Journal Article SB - IM
Abstract
Hyperinsulinism in infancy (HI) is a condition of neonates and early childhood. For many years the pathophysiology of this potentially lethal disorder was unknown. Advances in the genetics, histopathology and molecular physiology of this disease have now provided insights into the causes of beta-cell dysfunction and revealed levels of diversity far in excess of our previous knowledge. These include defects in ion channel subunit genes and mutations in several enzymes associated with beta-cell metabolism and anaplerosis. In most cases, beta-cell pathophysiology leads to an alteration in the function of ATP-sensitive K(+) channels. This can manifest as 'channelopathies' of K(ATP) channels through gene defects in ABCC8 and KCNJ11 (Ch.11p15); or as a result of 'metabolopathies' through defects in the genes encoding glucokinase (GCK, Ch.7p15-p13), glutamate dehydrogenase (GLUD1, Ch.10q23.3) and short-chain L-3-hydroxyacyl-CoA dehydrogenase (HADHSC, Ch.4q22-q26). This review focuses upon the relationship between the causes of HI and therapeutic options
Publication data is maintained in RPS. Visit https://rps.ucl.ac.uk
 More search options
UCL Researchers
Author
Infection, Immunity & Inflammation Dept
University College London - Gower Street - London - WC1E 6BT Tel:+44 (0)20 7679 2000

© UCL 1999–2011

Search by