Neurofibromatosis refers to a group of three distinct genetic conditions in which tumors grow in the nervous system. Most tumors are benign, but some are cancerous, and they often involve the skin or surrounding bone; symptoms are often mild, and each condition presents differently. Neurofibromatosis type I is typically characterized by cafe au lait spots, neurofibromas, scoliosis, and headaches; neurofibromatosis type II may present with early-onset hearing loss, cataracts, tinnitus, difficulty walking or maintaining balance, and muscle atrophy; and the third type, schwannomatosis, often presents in early adulthood with widespread pain, numbness, or tingling due to nerve compression.
Facts
Classification
ICD-10 ChapterVI: Diseases of the Nervous System 1 Communicable or Non-communicable Transmission Route Causative Agent
Causative Agent (category) First Described Sources
1. Wikipedia: ICD-10
WikipediaList of chapters, Chapter VIQuote, List of chapters, Chapter VI
Diseases of the nervous system
View the Source 2. Wikipedia: Non-communicable disease
WikipediaLead section, transmission-route statement (inferred from disease-category)
NCDs include Parkinson's disease, autoimmune diseases, strokes, heart diseases, cancers, diabetes, chronic kidney disease, osteoarthritis, osteoporosis, Alzheimer's disease, cataracts, and others.
Named examples section
NCDs include Parkinson's disease, autoimmune diseases, strokes, heart diseases, cancers, diabetes, chronic kidney disease, osteoarthritis, osteoporosis, Alzheimer's disease, cataracts, and others.
View the Source 3. Neurofibromatosis (Wikipedia)
lead paragraphQuote, lead paragraph
Neurofibromatosis (NF) refers to a group of three distinct genetic conditions in which tumors grow in the nervous system.
View the Source 4. Neurofibromatosis type I (Wikipedia)
Formally described by von Recklinghausen in 1882, article introView the Source Wikidata: Neurofibromatosis
Wikidata Q847605, class allow-list match (w-wdresolver-0926)View the Source Reader Challenges (0)
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