Figure of various morbidities associated with neurofibromatosis type II. The three types of neurofibromatosis are caused by different mutations on chromosomes...

Neurofibromatosis type I (NF-1), or von Recklinghausen syndrome, is a complex multi-system human disorder caused by the mutation of neurofibromin 1 (NF-1)...

Neurofibromatosis type II (also known as MISME syndrome – multiple inherited schwannomas, meningiomas, and ependymomas) is a genetic condition that may...

often mistaken for neurofibromatosis type I. It is caused by mutations in the SPRED1 gene. It is also known as neurofibromatosis type 1-like syndrome...

He made his acting debut in the 2013 film Under the Skin. He has neurofibromatosis and has been involved in outreach programmes to prevent bullying associated...

neurofibromatosis type 1. Epilepsy is seen in 4-7% of patients. Musculoskeletal system manifestations can develop in patients with neurofibromatosis type...

tell-tale sign of neurofibromatosis, multiple cafe au lait spots; however, testing of the gene usually involved in neurofibromatosis revealed it to be...

as neurofibromatosis type 1 and McCune–Albright syndrome. The size and shape of the spots can vary in terms of description. In neurofibromatosis type...

to Treat Children With Neurofibromatosis Type 1 and Progressive Plexiform Neurofibromas" Viskochil D (2010). "Neurofibromatosis 1: Current Issues in Diagnosis...

rare genetic disorder closely related to the more-common disorder neurofibromatosis (NF). Originally described in Japanese patients, it consists of multiple...