Congenital myasthenic syndrome in a cohort of patients with ‘double’ seronegative myasthenia gravis

BACKGROUND: Congenital myasthenic syndromes (CMS) have some phenotypic overlap with seronegative myasthenia gravis (SNMG). OBJECTIVE: The aim of this single center study was to assess the minimum occurrence of CMS misdiagnosed as double SNMG in a Brazilian cohort. METHODS: The genetic analysis of th...

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Detalles Bibliográficos
Autores principales: Lorenzoni, Paulo José, Ducci, Renata Dal-Pra, Arndt, Raquel Cristina, Hrysay, Nyvia Milicio Coblinski, Fustes, Otto Jesus Hernandez, Töpf, Ana, Lochmüller, Hanns, Werneck, Lineu Cesar, Kay, Cláudia Suemi Kamoi, Scola, Rosana Herminia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academia Brasileira de Neurologia -ABNEURO 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651496/
https://www.ncbi.nlm.nih.gov/pubmed/34932651
http://dx.doi.org/10.1590/0004-282X-ANP-2020-0575

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651496/
https://www.ncbi.nlm.nih.gov/pubmed/34932651
http://dx.doi.org/10.1590/0004-282X-ANP-2020-0575

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