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Bulbar dysfunction: An early presentation of congenital myasthenic syndrome in three infants
Congenital myasthenic syndromes are a group of rare genetic disorders affecting neuromuscular transmission. A high index of suspicion is required as clinical manifestations can be variable and nonspecific. Clinical phenotype includes arthrogryposis, respiratory crises, facial deformities, and weakne...
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| 主要な著者: | , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Medknow Publications & Media Pvt Ltd
2011
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3296406/ https://ncbi.nlm.nih.gov/pubmed/22408661 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1817-1745.92832 |
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