Takayasu's arteritis (aortic arch syndrome): Difference between revisions

m Text replacement - "reconcilled" to "reconciled"
m Text replacement - "Muscoloskeletal/soft" to "Musculoskeletal/soft"
Line 10: Line 10:
}}
}}


{{ICD10 category|Skin}}{{ICD10 category|Muscoloskeletal/soft tissue}}{{ICD10 category|Heme/immunology}}  
{{ICD10 category|Skin}}{{ICD10 category|Musculoskeletal/soft tissue}}{{ICD10 category|Heme/immunology}}  
== Additional Info ==
== Additional Info ==
*Takayasu arteritis is a rare, systemic, inflammatory large-vessel vasculitis of unknown etiology that most commonly affects women of childbearing age. It is defined as "granulomatous inflammation of the aorta and its major branches" by the Chapel Hill Consensus Conference on the Nomenclature of Systemic Vasculitis
*Takayasu arteritis is a rare, systemic, inflammatory large-vessel vasculitis of unknown etiology that most commonly affects women of childbearing age. It is defined as "granulomatous inflammation of the aorta and its major branches" by the Chapel Hill Consensus Conference on the Nomenclature of Systemic Vasculitis