PHILADELPHIA (WPVI) -- There's no cure for neurofibromatosis (NF), and it's been said that the rare genetic disorder is becoming more common. Now a local mother, who was born with the rare disease, is ...

In a major breakthrough, the Food and Drug Administration (FDA) has approved a treatment for a genetic disorder called neurofibromatosis type one (NF1). The disease impacts more than 2.5 million ...

It’s an invisible disease and a rare condition that starts in childhood. It’s a devastating diagnosis, but there is some new progress toward treatment neurofibromatosis — or NF. The first sign is a ...

The Food and Drug Administration has approved selumetinib for the treatment of pediatric patients aged 2 years and older with type 1 neurofibromatosis (NF1) with symptomatic, inoperable plexiform ...

Neurogenic tumour of the nasal cavity is a rare entity and it is rarer still for it to present with visual problem. We like to report a rare case of solitary nasal neurofibroma, which came to light ...