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A case of Satoyoshi's syndrome.

作者信息

Ikegawa S, Nagano A, Nakamura K, Kurokawa T

机构信息

Department of Orthopedics, Faculty of Medicine, University of Tokyo, Japan.

出版信息

J Pediatr Orthop. 1993 Nov-Dec;13(6):793-6. doi: 10.1097/01241398-199311000-00022.

DOI:10.1097/01241398-199311000-00022
PMID:8245211
Abstract

Satoyoshi's syndrome is a rare neurologic disorder characterized by progressive muscle spasms, alopecia, diarrhea, and skeletal abnormalities. We describe a 21-year-old woman with Satoyoshi's syndrome whose skeletal changes were followed for 15 years until after she had reached skeletal maturity. The patient developed slipping of the epiphyses in the proximal humeri and femurs and metaphyseal lesions mimicking metaphyseal chondrodysplasia. These lesions were a consequence of physeal injuries caused by the recurrent muscle spasms.

摘要

相似文献

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A case of Satoyoshi's syndrome.
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引用本文的文献

1
Gastrointestinal manifestations in Satoyoshi syndrome: a systematic review.Satoyoshi 综合征的胃肠道表现:系统评价。
Orphanet J Rare Dis. 2020 May 19;15(1):115. doi: 10.1186/s13023-020-01395-8.
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Treatment of Satoyoshi syndrome: a systematic review.治疗 Satoyoshi 综合征:系统评价。
Orphanet J Rare Dis. 2019 Jun 19;14(1):146. doi: 10.1186/s13023-019-1120-7.