Literature DB >> 14601924

A case of Satoyoshi syndrome: a multisystem disorder.

Deepak Kamat1, Laura Petry, Susan Berry.   

Abstract

A 14-year-old boy with Satoyoshi syndrome is reported. Less than 50 patients with Satoyoshi syndrome have been reported in the world literature. This patient had alopecia, muscle spasms, and skeletal abnormalities, which are three of the most common clinical features of Satoyoshi syndrome. Despite extensive laboratory evaluation, an alternate explanation was not documented for the cluster of clinical findings in this patient. Immune dysregulation is believed to be an underlying mechanism for the development of Satoyoshi syndrome. In contrast to some reports, this patient failed to respond to intravenous immunoglobulin therapy. However, he responded dramatically to steroids.

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Year:  2003        PMID: 14601924     DOI: 10.1177/000992280304200811

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN: 0009-9228            Impact factor:   1.168


  2 in total

1.  Adult-onset Satoyoshi syndrome and response to plasmapheresis.

Authors:  Rajeshwari Aghoram; P R Srijithesh; Sudheeran Kannoth
Journal:  Ann Indian Acad Neurol       Date:  2016 Jan-Mar       Impact factor: 1.383

Review 2.  Treatment of Satoyoshi syndrome: a systematic review.

Authors:  Julián Solís-García Del Pozo; Carlos de Cabo; Javier Solera
Journal:  Orphanet J Rare Dis       Date:  2019-06-19       Impact factor: 4.123

  2 in total

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