Abstract
A child with developmental delay and epilepsy developed glucosuria approximately 16 months after starting valproic acid therapy. Laboratory evaluation revealed global defects in proximal tubule function consistent with the De Toni-Debré-Fanconi syndrome. Discontinuation of valproate led to complete recovery 5 months later. Review of previously reported cases indicates that this complication is unique to children and reversible when the medication is discontinued.
| Original language | English |
|---|---|
| Pages (from-to) | 318-319 |
| Number of pages | 2 |
| Journal | Pediatric Neurology |
| Volume | 27 |
| Issue number | 4 |
| DOIs | |
| State | Published - Oct 2002 |
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