Neurofibromatosis Type I
Neurofibromatosis type 1 (NF1), also known as 'Von Recklinghausen’s disease', is a genetic disorder affecting about 1 in 3000 people. Physical manifestations of NF1 include:
skin fold freckling,
optic nerve glioma,
osseous (bone) abnormalities,
iris Lisch nodules,
and cutaneous and plexiform neurofibromas.
Cognitive impairment is present in approximately 50% of NF1 patients. Many different types of cognitive problems have been observed in NF1-patients. Our previous studies have focused on the further elucidation of the cognitive profile of NF1-patients.
We have extended this research to include aspects of social cognition and social functioning. Studies have also described many different abnormalities in the brains of NF1-patients, but have largely been unable to find strong associations with cognitive functioning. Our current work involves a study into structural and functional connectivity in the brains of NF1-patients in relation to their (social-) cognitive functioning.
This study is performed in collaboration with the Leiden Institute for Brain and Cognition (LIBC).
This research is supported by a grant/donation from the Dutch Neurofibromatosis Association (NFVN).