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  2. Campylobacteriosis - Wikipedia

    en.wikipedia.org/wiki/Campylobacteriosis

    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.

  3. Campylobacter jejuni - Wikipedia

    en.wikipedia.org/wiki/Campylobacter_jejuni

    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 ...

  4. CAPOS syndrome - Wikipedia

    en.wikipedia.org/wiki/CAPOS_syndrome

    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.

  5. Cerebellar ataxia, neuropathy, vestibular areflexia syndrome

    en.wikipedia.org/wiki/Cerebellar_ataxia...

    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.

  6. Campylobacter - Wikipedia

    en.wikipedia.org/wiki/Campylobacter

    [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 ...

  7. Kenny–Caffey syndrome - Wikipedia

    en.wikipedia.org/wiki/Kenny–Caffey_syndrome

    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.

  8. Bruce Willis' daughter Rumer shares rare update on how he's ...

    www.aol.com/news/bruce-willis-health-know...

    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 ...

  9. Primary ciliary dyskinesia - Wikipedia

    en.wikipedia.org/wiki/Primary_ciliary_dyskinesia

    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).