Takayasu's arteritis

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Noun1.Takayasu's arteritis - 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 ?
Clinical manifestations of Takayasu arteritis in India and Japan--new classification of angiographic findings.
Other conditions associated with pediatric PG include leukemia, IgA monoclonal gammopathy, Crohn's disease, rheumatoid arthritis, Takayasu disease and various immunodeficiency states including HIV, chronic granulomatous disease, and hyper IgE syndrome.
I hope he becomes as successful as Takayasu and Mitakeumi.
Takayasu arteritis (TA) is a chronic, recurrent, inflammatory vasculitis characterized by granulomatous inflammation in the vessel wall, and mainly affects young females.
Puede ser debido a iatrogenia, aterosclerosis, hipertension, tabaquismo, traumatismo, embarazo, displasia fibromuscular, enfermedad inflamatoria o infecciosa, enfermedad congenita de la pared vascular (sindrome de Ehlers-Danlos), degeneracion quistica de la capa media (sindrome de Marfan), o conectivopatias (arteritis de celulas gigantes, sindrome de Takayasu, poliarteritis).
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.
Takano Y, Fukuda K, Takayasu H, Shinmura K, Koizumi G, et al.
Esta complicacion, a diferencia de la arteritis de Takayasu, predomina en hombres, mayores de 50 anos y no asiaticos, y puede manifestarse como masa perivascular, aneurisma, diseccion o ruptura, en contraste con Takayasu donde predominan las estenosis.
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.
La arteritis de Takayasu es una vasculitis de grandes vasos de origen desconocido mediada por celulas T sin anticuerpos organo-especificos, aunque se describe de forma ocasional anticuerpos antiaorta, antiendotelio y antianexina V (1).
Sach Takayasu, President and CEO, Asian Pacific Islander American Chamber of Commerce