Neurofibromatosis, type 4, of Riccardi: A rare genetic disorder characterized by areas of increased and decreased skin pigmentation and the development of many non-cancerous nerve and skin tumors some of which may eventually become malignant. More detailed information about the symptoms, causes, and treatments of Neurofibromatosis, type 4, of Riccardi is available below.
See full list of 13 symptoms of Neurofibromatosis, type 4, of Riccardi
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Neurofibromatosis, type 4, of Riccardi is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Neurofibromatosis, type 4, of Riccardi, or a subtype of Neurofibromatosis, type 4, of Riccardi,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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