Abstract
We report a case with Klinefelter's Syndrome and early-onset childood epilepsy with occipital spikes (Panayotopoulos type). The karyotipe is 47, XXY in 89% of the mitoses and 48, XXYY in the rest of the cells (11%). The child experienced three crises between 5 and 8 years characterized by longlasting, eyes deviation, loss of consciousness, vomiting and right hemiconvulsions.
Translated title of the contribution | Klinefelter' syndrome and benign childood epilepsy with occipital spikes |
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Original language | Italian |
Pages (from-to) | 81-83 |
Number of pages | 3 |
Journal | Bollettino - Lega Italiana contro l'Epilessia |
Issue number | 118 |
Publication status | Published - Oct 2002 |
ASJC Scopus subject areas
- Clinical Neurology