Information on neurofibromatosis can be found online on reputable health websites, such as WebMD, Mayo Clinic, KidsHealth and National Institutes of Health. Alternatively, a person can consult a doctor to understand the condition in detail should there be a need. Visiting a doctor for more information is more important especially if a person suspects the occurrence of the condition.
Neurofibromatosis is a genetic disorder that affects the nervous system, resulting in the growth of tumors on the nerve tissue. It mainly affects the growth and development of nerve cells. The tumors usually sprout in the nervous system, including in the nerves, spinal cord and the brain.
There are three types of neurofibromatosis, including type 1 neurofibromatosis, type 2 neurofibromatosis and schwannomatosis. All these conditions are usually diagnosed depending on their specific symptoms, as stated by MedlinePlus.
The tumors are usually benign, but can be cancerous in some cases. Some symptoms of neurofibromatosis are learning impairment, hearing loss, poor balance, dizziness, bone deformities, cataracts, loss of vision, severe pain and severe disability, among others.
The condition can be diagnosed through different ways, such as physical examination, eye tests, genetic testing, family history, computer tomography scans, medical history, biopsy and magnetic resonance imaging. Depending on the symptoms, it can be treated though a surgical operation, medications and radiation therapy.