| Literature DB >> 23352578 |
Giuseppe d'Annunzio1, Marta Marchi, Concetta Aloi, Alessandro Salina, Francesca Lugani, Renata Lorini.
Abstract
We describe 10-year-old girl with mild incidental hyperglycaemia, impaired glucose tolerance and GADA positivity. Family history for mild hyperglycaemia and GADA fluctuation alerted us to a possible MODY diagnosis which was confirmed by detection of GCK mutation c.626C>T; p.T209M. Weak or transient β-cell autoimmunity should not preclude genetic testing for MODY when the clinical features are suggestive.Entities:
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Year: 2013 PMID： 23352578 DOI： 10.1016/j.diabres.2013.01.003
Source DB: PubMed Journal: Diabetes Res Clin Pract ISSN： 0168-8227 Impact factor: 5.602