Article
Electroclinical features of epilepsy monosomy 1p36 syndrome and their implications.
Acta neurologica Scandinavica - 1 Dec 2018
Verrotti Alberto, Greco Marco, Varriale Gaia, Tamborino Agnese, Savasta Salvatore, Carotenuto Marco, Elia Maurizio, Operto Francesca, Margari Lucia, Belcastro Vincenzo, Selicorni Angelo, Freri Elena, Matricardi Sara, Granata Tiziana, Ragona Francesca, Capovilla Giuseppe, Spalice Alberto, Coppola Giangennaro, Striano Pasquale
Abstract excerpt
OBJECTIVIES: Monosomy 1p36 syndrome is a recognized syndrome with multiple congenital anomalies; medical problems of this syndrome include developmental delay, facial dysmorphisms, hearing loss, short stature, brain anomalies, congenital heart defects. Epilepsy can be another feature but there are few data about the types of seizures and long term prognosis. The aim of this work was to analyse the electroclinical...
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