Since 2020, FIMARAD, the French healthcare network for rare dermatological diseases, has been supporting scientific innovation through its Research Call for Projects, aimed at identifying and funding research dedicated to rare dermatological diseases as well as improving their management.
In 2026, the project entitled “Identification of somatic mutations in the NF1 gene in fetuses affected by neurofibromatosis type 1” , led by Laura Fertitta and Laurence Pacot from CERENEF, was selected among eight successful projects.
This distinction highlights the scientific quality of this work as well as the commitment invested in bringing it to completion. Congratulations!