Satoyoshi syndrome
Satoyoshi syndrome is a very rare disorder of unknown etiology, characterized by progressive, intermittent, painful muscle spasms, alopecia universalis, diarrhea or unusual malabsorption, various endocrine disorders, and secondary skeletal abnormalities. This report describes a 9-year-old Thai girl...
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th-mahidol.266792018-09-07T16:45:17Z Satoyoshi syndrome Wanee Wisuthsarewong Supawadee Likitmaskul Jane Manonukul Mahidol University Medicine Satoyoshi syndrome is a very rare disorder of unknown etiology, characterized by progressive, intermittent, painful muscle spasms, alopecia universalis, diarrhea or unusual malabsorption, various endocrine disorders, and secondary skeletal abnormalities. This report describes a 9-year-old Thai girl who developed alopecia universalis when she was 6 years old. At age 7 years, she began to have recurrent, painful muscle spasms. The spasms progressed in time, producing recurrent patella dislocation. The laboratory investigations and radiologic study were compatible with Satoyoshi syndrome. She was treated with oral corticosteroid therapy, with marked improvement of her muscle spasms and alopecia. She underwent corrective surgery for deformities of both knees with a normal healing process. 2018-09-07T09:45:17Z 2018-09-07T09:45:17Z 2001-11-29 Article Pediatric Dermatology. Vol.18, No.5 (2001), 406-410 10.1046/j.1525-1470.2001.01966.x 07368046 2-s2.0-0035162191 https://repository.li.mahidol.ac.th/handle/123456789/26679 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0035162191&origin=inward |
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Mahidol University |
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Mahidol University Library |
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Asia |
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Thailand Thailand |
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Mahidol University Library |
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Mahidol University Institutional Repository |
| topic |
Medicine |
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Medicine Wanee Wisuthsarewong Supawadee Likitmaskul Jane Manonukul Satoyoshi syndrome |
| description |
Satoyoshi syndrome is a very rare disorder of unknown etiology, characterized by progressive, intermittent, painful muscle spasms, alopecia universalis, diarrhea or unusual malabsorption, various endocrine disorders, and secondary skeletal abnormalities. This report describes a 9-year-old Thai girl who developed alopecia universalis when she was 6 years old. At age 7 years, she began to have recurrent, painful muscle spasms. The spasms progressed in time, producing recurrent patella dislocation. The laboratory investigations and radiologic study were compatible with Satoyoshi syndrome. She was treated with oral corticosteroid therapy, with marked improvement of her muscle spasms and alopecia. She underwent corrective surgery for deformities of both knees with a normal healing process. |
| author2 |
Mahidol University |
| author_facet |
Mahidol University Wanee Wisuthsarewong Supawadee Likitmaskul Jane Manonukul |
| format |
Article |
| author |
Wanee Wisuthsarewong Supawadee Likitmaskul Jane Manonukul |
| author_sort |
Wanee Wisuthsarewong |
| title |
Satoyoshi syndrome |
| title_short |
Satoyoshi syndrome |
| title_full |
Satoyoshi syndrome |
| title_fullStr |
Satoyoshi syndrome |
| title_full_unstemmed |
Satoyoshi syndrome |
| title_sort |
satoyoshi syndrome |
| publishDate |
2018 |
| url |
https://repository.li.mahidol.ac.th/handle/123456789/26679 |
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1763489606309773312 |