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A rare disease is any disease that affects a small percentage of the population. In some parts of the world, the term orphan disease describes a rare disease whose rarity results in little or no funding or research for treatments, without financial incentives from governments or other agencies. Orphan drugs are medications targeting orphan ...
Familial Alzheimer-like prion disease; Febrile infection-related epilepsy syndrome; Felty's syndrome; Fetal hydantoin syndrome; Fetal trimethadione syndrome; FG syndrome; Fitz-Hugh–Curtis syndrome; Fitzsimmons–Guilbert syndrome; Fleischer's syndrome; Floating–Harbor syndrome; Fountain syndrome; Franceschetti–Klein syndrome; Frank–Ter ...
It should directly contain very few, if any, pages and should mainly contain subcategories. The main article for this category is rare disease . A rare disease is technically defined (in the European Union) as a disease that is found in fewer than 5 people per every 10,000 people.
Fortunately, Bayliscacaris infection in humans is extremely rare. As the CDC noted in a September 9 report on seven cases (none fatal) detected between 2013 and 2015, the United States saw just 22 ...
Fibrodysplasia ossificans progressiva (/ ˌ f aɪ b r oʊ d ɪ ˈ s p l eɪ ʒ (i) ə ɒ ˈ s ɪ f ɪ k æ n z p r ə ˈ ɡ r ɛ s ɪ v ə /; [1] abbr. FOP), also called Münchmeyer disease or formerly myositis ossificans progressiva, is an extremely rare connective tissue disease in which fibrous connective tissue such as muscle, tendons, and ligaments turn into bone tissue (ossification).
Fields condition, [1] also known as Fields' disease, [2] [3] is a neuromuscular disease that is considered the rarest medical condition in the world. It was named after Welsh identical twins Catherine and Kirstie Fields, who are two of only three people known to have been affected.
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