Abstract
We report the diagnosis of Sandifer syndrome in a neurodevelopmentally normal 16-month old boy with a history of atypical "absences" refractory to Valproate, Ethosuccimide or Clonazepam therapy and associated with a normal electroencephalogram (EEG). Videotaping of these episodes by his parents was crucial for the diagnosis and the associated gastroesophageal reflux (GER) was confirmed by esophageal pH studies and the presence of free GER. Following antireflux therapy his symptoms resolved entirely. Children with torticollis, dystonic posturing or atypical seizures should be evaluated for GER. Exhaustive neurologic investigations and anticonvulsant therapy are unnecessary.
Original language | English |
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Pages (from-to) | 39-41 |
Number of pages | 3 |
Journal | International Pediatrics |
Volume | 19 |
Issue number | 1 |
Publication status | Published - 2004 |
Externally published | Yes |
Keywords
- Gastroesophageal reflux
- Sandifer syndrome
- Seizures
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health