Genetic testing for maturity onset diabetes of the young in childhood hyperglycaemia. Issue 6 (1st June 1998)

• Record Type: Journal Article
• Authors: Matyka, K A; Beards, F; Appleton, M; Ellard, S; Hattersley, A; Dunger, D B
• Is Part Of: Archives of disease in childhood. Volume 78:Issue 6(1998)
• Page Start: 552
• Page End: 554
• Publication Date: 1998-06-01
• Subjects: maturity onset diabetes of the young -- hyperglycaemia -- DNA sequencing -- mutation; Children -- Diseases -- Periodicals; Infants -- Diseases -- Periodicals; 618.920005
• DOI: 10.1136/adc.78.6.552
• Languages: English
• ISSNs: 0003-9888

Abstract

Abstract : Mild hyperglycaemia is a common finding during minor illness in children. The differential diagnosis includes maturity onset diabetes of the young (MODY), which can be a difficult diagnosis to make clinically. As most genes resulting in MODY have been identified, it is possible to make a firm diagnosis using mutation detection. A case is reported of a 4 year old girl in whom a diagnosis of MODY2 was established by the finding of a heterozygous missense mutation in exon 7 of the glucokinase gene, resulting in the substitution at codon 259 of alanine by threonine (A259T). Observations from other glucokinase families suggest that hyperglycaemia in this child is likely to be stable and will not require intensive medical follow up, whereas other forms of MODY (1, 3, and 4) might carry a different prognosis.