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An outbreak of human monkeypox (now known as mpox) began in May 2003 in the United States.By July, a total of 71 cases were found in six Midwestern states including Wisconsin (39 cases), Indiana (16), Illinois (12), Kansas (1), Missouri (2), and Ohio (1).
Widespread non-communicable diseases such as cardiovascular disease and cancer are not included. An epidemic is the rapid spread of disease to a large number of people in a given population within a short period of time; in meningococcal infections , an attack rate in excess of 15 cases per 100,000 people for two consecutive weeks is considered ...
A rare disease is technically defined ... as a disease that is found in fewer than 5 people per every 10,000 people. ... Statistics; Cookie statement; Mobile view;
Bradley received a diagnosis faster because of his father, but Elly said they still wanted to rule out every other possibility. CJD – while rare – is the most common prion disease in humans ...
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).
The disease proved to be the cause of death of one of the patients, the other also had circulatory failure. The bacteria responsible for legionellosis was found in four patients from this hospital. [24] In total the outbreak resulted in three deaths [25] 2008: New Brunswick, New Jersey, United States: Saint Peter's University Hospital: Drinking ...
Rare diseases caused by infectious agents rather than genetic or environmental factors. Pages in category "Rare infectious diseases" The following 46 pages are in this category, out of 46 total.
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.