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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Detalles Bibliográficos
Autores principales: Khan, Arif, Hussain, Nahin, Gosalakkal, Jayaprakash A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296406/
https://www.ncbi.nlm.nih.gov/pubmed/22408661
http://dx.doi.org/10.4103/1817-1745.92832

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296406/
https://www.ncbi.nlm.nih.gov/pubmed/22408661
http://dx.doi.org/10.4103/1817-1745.92832

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