Neurofibroma (patient information)
For the WikiDoc page for this topic, click here
Editor-in-Chief: Jinhui Wu, MD
Please Join in Editing This Page and Apply to be an Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
What is neurofibroma?
Neurofibroma is genetic disorders of the nervous system that result in the growth of noncancerous tumors along nerves. There are two main forms of neurofibroma: peripheral neurofibromatosis and central neurofibromatosis.
How do I know if I have neurofibroma and what are the symptoms of neurofibroma?
Severity of symptoms varies greatly. It depends on the nerve infiltrated.
Who is at risk for neurofibroma?
Studies suggested that the cause of neurofibroma is related to gene mutations.
How to know you have neurofibroma?
When to seek urgent medical care?
Treatment options
Diseases with similar symptoms
Where to find medical care for neurofibroma?
Directions to Hospitals Treating neurofibroma
Prevention of neurofibroma
Because the risk factor is not clear, the preventive measure is unknown.