We report the case of a 6-year-2-month-old female affected by trisomy 12p syndrome. Seizures were typical myoclonic absences from both the clinical and EEG points of view. Our patient and other sporadic reports in the literature seem to support the hypothesis that, at least in some cases, myoclonic absences can be a direct or indirect effect of a chromosomopathy. (C) 1998 Elsevier Science B.V.

Trisomy 12p and epilepsy with myoclonic absences

Elia M;
1998-01-01

Abstract

We report the case of a 6-year-2-month-old female affected by trisomy 12p syndrome. Seizures were typical myoclonic absences from both the clinical and EEG points of view. Our patient and other sporadic reports in the literature seem to support the hypothesis that, at least in some cases, myoclonic absences can be a direct or indirect effect of a chromosomopathy. (C) 1998 Elsevier Science B.V.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11387/192593
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