Literature DB >> 6684258

Myasthenia gravis associated with Satoyoshi syndrome: muscle cramps, alopecia, and diarrhea.

A Satoh, M Tsujihata, T Yoshimura, M Mori, S Nagataki.   

Abstract

We studied a woman who had evidence of myasthenia gravis at age 17. At age 19, she gradually developed alopecia and painful muscle spasms (Satoyoshi disease). Deposition of immune complexes (IgG, C3, and C9) was demonstrated at the motor endplates of limb muscle (biceps brachii); primary synaptic clefts were widened, and postsynaptic folds were simplified. This is the first case of myasthenia and Satoyoshi disease in the same patient.

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Year:  1983        PMID: 6684258     DOI: 10.1212/wnl.33.9.1209

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  3 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.  Gastrointestinal manifestations in Satoyoshi syndrome: a systematic review.

Authors:  Julián Solís-García Del Pozo; Carlos de Cabo; Javier Solera
Journal:  Orphanet J Rare Dis       Date:  2020-05-19       Impact factor: 4.123

Review 3.  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

  3 in total

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