Miastenia Gravis
نویسندگان
چکیده
Objetivo: Analisar as características da Miastenia Gravis (MG). Revisão bibliográfica: A MG é uma doença autoimune mediada por anticorpos que afeta a membrana pós-sináptica na junção neuromuscular, sendo produzida diferentes contra proteínas sináptica. Isso, geralmente, em mais de 85% dos casos causado um tipo anticorpo o receptor acetilcolina do músculo esquelético (AChR-ab). rara; incidência anual estimada 1 2 100.000, e sua prevalência mundial 150 250 milhão indivíduos. Considerações finais: distúrbio neuromuscular cuja principal característica clínica fraqueza flutuante tem piora ao exercício melhora com repouso. Seu diagnóstico clínico, laboratorial sorologias para os associados à partir exames como eletromiografia. terapêutica envolve controle sintomas Piridostigmina modulação terapias imunossupressoras esteróides não esteróides. Atualmente, há, ainda, opção utilizar imunoglobulina intravenosa troca plasma.
منابع مشابه
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A case of myasthenia gravis in a 15 years old girl is pre·sented. The disease was present for 5 years before thymectomy was performed. Indications for thymectomy, preoperative preparation, anesthetic and surgical management is -discussed.
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Congenital myasthenia gravis is caused by genetic mutations affecting neuromuscular transmission, characterized by muscle weakness usually starting in childhood. A two and a half years old male child presented with bilateral ptosis and hoarseness of voice. The symptoms progressed giving the clinical impression of congenital myasthenia gravis. A series of tests were done including Ice Pack Test,...
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ژورنال
عنوان ژورنال: Revista Eletrônica Acervo Saúde
سال: 2023
ISSN: ['2178-2091']
DOI: https://doi.org/10.25248/reas.e12726.2023