Neurofibromatose de type 1 : quels signes doivent alerter ?

Neurofibromatosis type 1, also known as NF1, is a genetic disorder that remains largely unknown. It can manifest in childhood, sometimes with visible signs such as café-au-lait spots on the skin, but also with other, more subtle symptoms. During Neurofibromatosis type 1 Awareness Month, Dr. Vaessen, a pediatric neurologist at the University Hospital of Liège and the Citadelle Hospital, explains the essential information needed to better understand this disease, recognize the early signs, and support those affected. In this video, she discusses: • what neurofibromatosis type 1 is; • the signs that can appear in children; • the possible manifestations affecting the skin, vision, bones, and learning; • the importance of early diagnosis; • medical follow-up and support for patients and their families. A better understanding of NF1 allows for faster detection, more appropriate monitoring, and better care when needed. This video was produced with Dr. Vaessen, a pediatric neurologist at the University Hospital of Liège and the Citadelle Hospital, in collaboration with Merck Healthcare.