Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals

Conclusion
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.

Source: Journal of Medical Genetics - March 21, 2024 Category: Genetics & Stem Cells Authors: Koene, S., Ropers, F. G., Wieland, J., Rybak, T., Wildschut, F., Berghuis, D., Morgan, A., Trelles, M. P., Scheepe, J. R., Bökenkamp, R., Peeters-Scholte, C. M. P. C. D., Braden, R., Santen, G. W. E. Tags: Phenotypes Source Type: research