pulseless disease

(redirected from Takayasu arteritis)
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Noun1.pulseless disease - disorder characterized by the absence of a pulse in both arms and in the carotid arteries
arteritis - inflammation of an artery
References in periodicals archive ?
b) positive results in Phase 2 or 3 trial, (c) proof of concept obtained, (d) no positive results in Phase 2 or 3, RA: rheumatoid arthritis, JIA: juvenile idiopathic arthritis, CD: Crohn's disease, UC: ulcerative colitis, AS: ankylosing spondylitis, SpA: spondyloathritis, PS: psoriasis, PsA: psoriatic arthritis, CAPS: cryopyrin associated periodic syndrome, FMF: familial medetrian fever, SLE: systemic lupus erythematosus, pSS: primary Sjogren's syndrome, SSc: systemic sclerosis, CCA: giant cell arthritis, TA: Takayasu arteritis, AAV: ANCA associated vasculitis, AOSD: adult-onset Still's disease
Clinical manifestations of Takayasu arteritis in India and Japan--new classification of angiographic findings.
Takayasu arteritis (TA) is a chronic, recurrent, inflammatory vasculitis characterized by granulomatous inflammation in the vessel wall, and mainly affects young females.
Takayasu arteritis (TA) is a medium and large vessel vasculitis of unknown etiology characterized by chronic granulomatous inflammation of the vessel wall leading to thickening, stenosis, dilatation, and/or aneurysm of the affected vessel.
Funding for robotic surgery, targeted radiotherapy for renal, spinal and pelvic cancer and medication for a rare condition called Takayasu arteritis, which causes swelling of blood vessels, is in peril.
Background: Takayasu arteritis (TA) is a rare inflammatory arteriopathy of unknown etiology.
Numano F, The story of Takayasu arteritis, Rheumatol.
These classification criteria were developed for HSP, childhood polyarteritis nodosa (PAN), Takayasu arteritis (TA) and granulomatous polyarteritis (GPA).
Takayasu arteritis most often occurs in women between the ages of 15 and 45 years, whereas giant cell arteritis is most commonly diagnosed in patients older than 50 years.
He also discussed about calcium pyrophosphate disease, Takayasu arteritis, Sjogren syndrome which increases the risk of developing lymphoma.
4) The acquired form of coarctation of aorta is commonly associated with inflammatory conditions like Takayasu arteritis (5) and severe atherosclerosis.