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.
Original language | English |
---|---|
Journal | Diabetes Research and Clinical Practice |
Volume | 100 |
Issue number | 1 |
DOIs | |
Publication status | Published - Apr 2013 |
Keywords
- β-Cell antibodies
- Hyperglycaemia
- MODY
- Pre-type 1 diabetes
ASJC Scopus subject areas
- Endocrinology, Diabetes and Metabolism
- Internal Medicine
- Endocrinology