This form of disease is frequently found with Takayasu's arteritis.

It is also commonly used for long term monitoring in Takayasu's arteritis.

Takayasu's arteritis appears to have an independent link to B52 associated disease.

Takayasu's arteritis appears to have a link to B39.

Angiography is commonly used for the diagnosis of Takayasu's arteritis.

The great majority of patients with Takayasu's arteritis respond to steroids such as prednisone.

B39 is suggested as a factor in Takayasu's arteritis and gallstones in Mexico.

Takayasu's arteritis is similar to other forms of vasculitis, including giant cell arteritis.

Some patients with Takayasu's arteritis may present with only late vascular changes, without an antecedent systemic illness.

Takayasu's arteritis is an inflammatory disease that mainly affects the larger vessels such as the aorta and its surrounding branches.

Takayasu's arteritis, disorder of the aorta.

Giant cell arteritis, polymyalgia rheumatica, and Takayasu's arteritis.

Education and support for persons with Takayasu's arteritis (an inflammation of the large elastic arteries and aorta), their families and health professionals.

However, in Takayasu's arteritis, where the aorta may be involved, it is unlikely a biopsy will be successful and angiography can be diagnostic.

Giant cell arteritis includes two types, these are Temporal arteritis and Takayasu's arteritis.

In the Western world, atherosclerosis is a more frequent cause of obstruction of the aortic arch vessels than Takayasu's arteritis.

MRA is used to diagnose early stages of Takayasu's arteritis, such as the thickening of the vessel wall.

One rare but important feature of the Takayasu's arteritis is ocular involvement in form of visual field defects, vision loss, or retinal hemorrhage.

Aortitis is most commonly seen in patients with syphilis, autoimmune vasculitis, giant cell arteritis, Takayasu's arteritis, and rheumatoid arthritis.

Takayasu's arteritis, polyarteritis nodosa and giant cell arteritis mainly involve arteries and are thus sometimes classed specifically under arteritis.

The first case of Takayasu's arteritis was described in 1908 by Japanese ophthalmologist Mikito Takayasu at the Annual Meeting of the Japan Ophthalmology Society.

Even rarer problems are an inflammation of the arteries called Takayasu's arteritis, and multiple narrowings of different arteries, first seen in Polynesians and called Moya-Moya syndrome.

Churg Strauss Syndrome Vasculitis, Cutaneous Necrotizing Managing Vasculitis Pain What Is Takayasu's Arteritis?

Anti-endothelial antibodies are associated with Takayasu's arteritis and anti-neutrophil cytoplasmic antibodies with macroscopic and microscipic polyarteritis nodosa or with Churg-Strauss syndrome.

Giant-cell arteritis and Takayasu's arteritis have much in common, but usually affect patients of different ages, with Takayasu's arteritis affecting younger people, and giant-cell arteritis having a later age of onset.