Tarsal-tunnel syndrome, a presenting feature of rheumatoid arthritis.
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چکیده
منابع مشابه
Tarsal-tunnel syndrome, a presenting feature of rheumatoid arthritis.
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متن کاملExtensive Osteochondroma of Talus Presenting as Tarsal Tunnel Syndrome: Report of a case and Literature Review
Osteochondroma or exostosis is the most common benign bone tumor, and occurring frequently in the proximal humerus, tibia, and distal femur. It rarely affects talus. Osteochondroma of talus is a very rare etiology of tarsal tunnel syndrome (TTS). We report a rare case of extensive osteochondroma of the talus in a 60 year old female presenting with multiple swellings around the ankle and sympt...
متن کاملTarsal-tunnel syndrome.
In 14 patients tarsal tunnel syndrome was associated with varus heels and pronated, splayed forefeet. Review of the literature and the author's experience suggest that these conditions may be a common cause of the tarsal tunnel syndrome. Treatment of fixed varus deformities of the heel by outer heel wedges has been shown to be ineffective. Although outer heel wedges provide symptomatic relief i...
متن کاملTarsal Tunnel Syndrome
The tarsal tunnel syndrome consists of a complex of symptoms affecting the foot and is thought to be due to a compression neuropathy of the posterior tibial nerve within the fibro-osseous “ tunnel “ that lies beneath the flexor retinaculum on the medial side of the ankle. No comprehensive description of this condition can be found until 1962, when two isolated cases were reported (Keck 1962, La...
متن کاملOccupational tarsal tunnel syndrome.
Tarsal tunnel syndrome characterises a complex of symptoms that result from compression of the posterior tibial nerve as it passes through the fibro-osseus tunnel located beneath the flexor retinaculum on the medial aspect of the ankle.' The syndrome has been described in several case reports and review articles24 since Keck's5 and Lam's6 original case reports in 1962. Whereas other nerve entra...
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ژورنال
عنوان ژورنال: BMJ
سال: 1970
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.3.5713.32