Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals.
Saskia KoeneFabiënne Gwendolin RopersJannelien WielandTamara RybakFloor WildschutDagmar BerghuisAngela T MorganMaria Pilar TrellesJeroen Ronald ScheepeRegina BökenkampCacha M P C D Peeters-ScholteRuth BradenGijs W E SantenPublished in: Journal of medical genetics (2024)
The results of this study may be used to further guide medical management and identify patient priorities for future research targeted on those features of FOXP1 syndrome that most impair quality of life of patients and their families.