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Campylobacteriosis is among the most common infections caused by a bacterium in humans, often as a foodborne illness. It is caused by the Campylobacter bacterium, [2] most commonly C. jejuni. It produces an inflammatory, sometimes bloody, diarrhea or dysentery syndrome, and usually cramps, fever and pain.
Serious systemic illness caused by campylobacter infection rarely occurs, but can lead to sepsis and death. The case-fatality rate for campylobacter infection is 0.05 per 1000 infections. For instance, one major possible complication that C. jejuni can cause is Guillain–Barré syndrome, which induces neuromuscular paralysis in a sizeable ...
CAPOS syndrome is a rare genetic neurological disorder which is characterized by abnormalities of the feet, eyes and brain which affect their normal function. These symptoms occur episodically when a fever-related infection is present within the body.
Cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) is an autosomal recessive late-onset heredodegenerative multisystem neurological disease. The symptoms include poor balance and difficulty walking. Chronic cough and difficulty swallowing may also be present.
[citation needed] Campylobacter has, on rare occasions, been suggested to cause hemolytic uremic syndrome [32] and thrombotic thrombocytopenic purpura, [33] though no unequivocal case reports exist. Campylobacter infection is the most common trigger of Guillain–Barré syndrome. [34] Gastrointestinal perforation is a rare complication of ileal ...
Kenny–Caffey syndrome type 2 (KCS2) is an extremely rare autosomal dominant genetic condition characterized by dwarfism, farsightedness, microphthalmia, and skeletal abnormalities. [1] This subtype of Kenny–Caffey syndrome is caused by a heterozygous mutation in the FAM111A gene (615292) on chromosome 11q12.
Cleveland Clinic said the life expectancy is seven and half years, while Barmada told TODAY.com that 10 years or longer is considered a good prognosis. This article was originally published on ...
When accompanied by the combination of situs inversus (reversal of the internal organs), chronic sinusitis, and bronchiectasis, it is known as Kartagener syndrome [3] (only 50% of primary ciliary dyskinesia cases include situs inversus).