Polyarteritis nodosa: A serious blood vessel disease where small and medium-sized arteries become swollen and damaged and are unable to adequately supply oxygenated blood to various tissues in the body. The disease can occur in a mild form or a serious, rapidly fatal form. More detailed information about the symptoms, causes, and treatments of Polyarteritis nodosa is available below.
See full list of 38 symptoms of Polyarteritis nodosa
Read more about treatments for Polyarteritis nodosa
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See full list of 7 causes of Polyarteritis nodosa
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Prognosis for Polyarteritis nodosa: death often occurs within a year in acute cases
More about prognosis of Polyarteritis nodosa
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The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Polyarteritis nodosa include:
See full list of 6 Clinical Trials for Polyarteritis nodosa
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Form of necrotizing vasculitis involving small- and medium-sized arteries; signs and symptoms result from infarction and scarring of the affected organ system. - (Source - Diseases Database)
A progressive disease of connective tissue that is characterized by nodules along arteries; nodules may block the artery and result in inadequate circulation to the particular area - (Source - WordNet 2.1)
Polyarteritis nodosa is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Polyarteritis nodosa, or a subtype of Polyarteritis nodosa,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Polyarteritis nodosa as a "rare disease".
Source - Orphanet
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