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...

Повний опис

Бібліографічні деталі

Автори:	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
Формат:	Artigo
Мова:	Inglês
Опубліковано:	Frontiers Media S.A. 2023-07-01
Серія:	Frontiers in Neurology
Предмети:	autism epilepsy movement disorder angiomas choanal atresia FOXP1
Онлайн доступ:	https://www.frontiersin.org/articles/10.3389/fneur.2023.1207176/full
Теги:	Додати тег Немає тегів, Будьте першим, хто поставить тег для цього запису!