Prolonged prodrome, systemic vasculitis, and deafness in Cogan's syndrome
نویسندگان
چکیده
منابع مشابه
Prolonged prodrome, systemic vasculitis, and deafness in Cogan’s syndrome
Cogan’s syndrome is a rare, multisystem disease which occurs predominantly in children and young adults. It was originally described as the combination of interstitial keratitis and audiovestibular disturbance, but other forms of ocular disease, as well as systemic vasculitis, have since been recognised as part of the syndrome. Diagnosis can be diYcult if the various manifestations occur separa...
متن کاملProlonged prodrome, systemic vasculitis, and deafness in Cogan's syndrome.
Cogan's syndrome is a rare, multisystem disease which occurs predominantly in children and young adults. It was originally described as the combination of interstitial keratitis and audiovestibular disturbance, but other forms of ocular disease, as well as systemic vasculitis, have since been recognised as part of the syndrome. Diagnosis can be difficult if the various manifestations occur sepa...
متن کاملChurg-Strauss syndrome: a rare systemic vasculitis.
Churg-Strauss syndrome is a rare diffuse small/medium sized vessel vasculitis that is almost invariably accompanied by severe asthma. The cause is unknown, but its characteristic histological findings and association with asthma distinguish it from other vasculitides. We report here a middle aged lady who presented with sudden onset of vasculitic skin lesions in association with long standing a...
متن کاملCogan's syndrome: a rare systemic vasculitis.
A 4 year old girl presented with keratitis and ataxia. Over the next two months she developed profound hearing loss, arthritis, and polychondritis. A diagnosis of Cogan's syndrome was made. The literature on the condition is reviewed and the importance of early diagnosis to prevent hearing loss is highlighted.
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Admas-Oliver syndrome is a rare autosomal dominant disease of congenital development defects association with aplasia cutis. All of 81 reported cases were of 32 group families. These two cases had congenital scalp cutis aplasia with developmental defect and hypoplasia of left foot digits in case 1.Congenital deaf-mute in both can added to the past known findings in this syndrome. Thoracic defor...
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ژورنال
عنوان ژورنال: Annals of the Rheumatic Diseases
سال: 2001
ISSN: 0003-4967
DOI: 10.1136/ard.60.1.69