Abstract
In Rett syndrome (RS), acute life-threatening episodes (ALTEs) are usually attributed to epilepsy or autonomic dysfunction but they can represent a movement disorder (MD). We describe three girls with RS who experienced ALTEs from an early age. These were long considered epileptic until video-EEG in Patients 1 and 3 revealed their non-epileptic nature. A primary dystonic mechanism was suspected and Patients 1 and 2 were treated with Trihexyphenidyl with significantly reduced frequency of the ALTEs. Patient 3 died before Trihexyphenidyl was tried. Trihexyphenidyl in RS patients with similar presentations can modify the dystonia and prevent ALTEs.
Original language | English |
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Pages (from-to) | 385-389 |
Number of pages | 5 |
Journal | Movement Disorders |
Volume | 25 |
Issue number | 3 |
DOIs | |
Publication status | Published - 15 Feb 2010 |
Keywords
- Rett syndrome
- dystonia
- epilepsy
- acute life threatening episodes
- trihexyphenidyl