Other Orphan Diseases 2018
DOI: 10.1136/annrheumdis-2018-eular.3542
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AB1134 Determining factors of severity in hemophilic arthropathy

Abstract: BackgroundIn patients with haemophilia, the development of inhibitors to factor VIII/IX (Haemophilia A and B, HA/HB), prevents adequate replacement therapy and results in increased risk of serious bleeding episodes, poor control of joint bleeding, and progressive, debilitating joint disease.ObjectivesTo describe, according to the Arnold-Hilgartner scale (AHRS), the radiological findings in a cohort of hemophilic arthropathy (HArth) patients and to analyse the relationship that may exist between the degree of j… Show more

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