Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Adicionar filtros








Intervalo de ano
1.
Rev. méd. Maule ; 34(2): 30-40, dic. 2019. tab
Artigo em Espanhol | LILACS | ID: biblio-1371248

RESUMO

Myasthenia gravis is an acquired autoimmune disorder of the neuromuscular junction characterized by fluctuating weakness and fatigability of skeletal muscles. The diagnosis can be established by clinical and serologic testing, with predominance of autoantibodies against the acetylcholine receptor, and Muscle-specific kinase antibodies. We report two cases of Myasthenia gravis, the first one is a 31 year old patient with a debut of the disease, mainly with bulbar symptoms, and the second one is a 29 year old patient diagnosed with generalized Miasthenia Gravis also mainly with bulbar symptoms with worsening of symptomatology. In this report treatments alternatives and management approaches are discused


Assuntos
Humanos , Feminino , Adulto , Miastenia Gravis/imunologia , Miastenia Gravis/tratamento farmacológico , Brometo de Piridostigmina/uso terapêutico , Timectomia , Imunoglobulinas Intravenosas/uso terapêutico , Glucocorticoides/uso terapêutico , Imunossupressores/uso terapêutico , Imunoterapia , Miastenia Gravis/cirurgia , Miastenia Gravis/classificação
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA