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A novel heterozygous mutation in the SLC5A2 gene causing severe glycosuria, mild failure to thrive, and subclinical
Dimitrios T Papadimitriou1,2, Emmanouil Manolakos3, Eleni Dermitzaki1
1Department of Pediatric-Adolescent Endocrinology & Diabetes, Athens Medical Center, Athens, Greece.
Abstract:
Highlights A novel heterozygous mutation in the SLC5A2 gene in a 2-year-old girl with severe asymptomatic glycosuria, mild failure to thrive, and subclinical hypoglycemia: Continuous glucose monitoring identified 14% hypoglycemic excursions (< 70 mg/dl), reduced at 1% with 1 g/Kg uncooked cornstarch at bed-time milk and eliminated (0%) adjusting the dose at 1.5 g/Kg, as shown by Flash technology.
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