Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures

ObjectiveWe aimed to report on previously unappreciated clinical features associated with FOXP1-related intellectual disability (ID) syndrome, a rare neurodevelopmental disorder characterized by global developmental delay, intellectual disability, and language delay, with or without autistic feature...

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Bibliografski detalji

Glavni autori:	Carlo Alberto Cesaroni, Marzia Pollazzon, Cecilia Mancini, Susanna Rizzi, Camilla Cappelletti, Simone Pizzi, Daniele Frattini, Carlotta Spagnoli, Stefano Giuseppe Caraffi, Roberta Zuntini, Gabriele Trimarchi, Marcello Niceta, Francesca Clementina Radio, Marco Tartaglia, Livia Garavelli, Carlo Fusco
Format:	Artigo
Jezik:	Inglês
Izdano:	Frontiers Media S.A. 2023-07-01
Serija:	Frontiers in Neurology
Teme:	autism epilepsy movement disorder angiomas choanal atresia FOXP1
Online pristup:	https://www.frontiersin.org/articles/10.3389/fneur.2023.1207176/full
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