Relapsing Polychondritis: Difference between revisions
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Relapsing polychondritis (RP) is a rare multisystem autoimmune disease of unknown origin characterized by recurrent episodes of inflammation and progressive destruction of cartilaginous tissues.<br> | Relapsing polychondritis (RP) is a rare multisystem autoimmune disease of unknown origin characterized by recurrent episodes of inflammation and progressive destruction of cartilaginous tissues.<br> | ||
== | == Etiology == | ||
The etiology of RP remains unknown so far. Studies have shown the association of both cellular immunity changes and abnormal autoantibody response in RP.<br> | |||
== Clinical Presentation == | == Clinical Presentation == | ||
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<references /> | <references /> | ||
[[Category:Autoimmune Disorders]] | [[Category:Autoimmune Disorders]] | ||
[[Category:Rheumatology]] |
Revision as of 08:26, 2 September 2023
Top Contributors - Pacifique Dusabeyezu, Kim Jackson and Carina Therese Magtibay
Clinically Relevant Anatomy
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Relapsing polychondritis (RP) is a rare multisystem autoimmune disease of unknown origin characterized by recurrent episodes of inflammation and progressive destruction of cartilaginous tissues.
Etiology[edit | edit source]
The etiology of RP remains unknown so far. Studies have shown the association of both cellular immunity changes and abnormal autoantibody response in RP.
Clinical Presentation[edit | edit source]
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Diagnostic Procedures[edit | edit source]
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Outcome Measures[edit | edit source]
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Management / Interventions
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Differential Diagnosis
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Resources
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