Forkhead Box G1 (FOXG1) syndrome is a developmental encephalopathy characterized by postnatal microcephaly, structural brain abnormalities, facial dysmorphisms, severe delay with absent language, defective social interactions, and epilepsy. Abnormal movements in FOXG1 syndrome have often been mentioned but not characterized.

The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy / Cellini, Elena; Vignoli, Aglaia; Pisano, Tiziana; Falchi, Melania; Molinaro, Anna; Accorsi, Patrizia; Bontacchio, Alessia; Pinelli, Lorenzo; Giordano, Lucio; Guerrini, Renzo. - In: DEVELOPMENTAL MEDICINE & CHILD NEUROLOGY. - ISSN 1469-8749. - STAMPA. - 58:(2016), pp. 93-97. [10.1111/dmcn.12894]

The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy

GUERRINI, RENZO
2016

Abstract

Forkhead Box G1 (FOXG1) syndrome is a developmental encephalopathy characterized by postnatal microcephaly, structural brain abnormalities, facial dysmorphisms, severe delay with absent language, defective social interactions, and epilepsy. Abnormal movements in FOXG1 syndrome have often been mentioned but not characterized.
2016
58
93
97
Cellini, Elena; Vignoli, Aglaia; Pisano, Tiziana; Falchi, Melania; Molinaro, Anna; Accorsi, Patrizia; Bontacchio, Alessia; Pinelli, Lorenzo; Giordano, Lucio; Guerrini, Renzo
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1044486
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