Severe progression of a young-onset non-paraneoplastic Lambert-Eaton myasthenic syndrome

The Lambert-Eaton Myasthenic Syndrome (LEMS) is a rare neuromuscular disorder characterized by proximal muscle weakness, hyporeflexia or areflexia, and dysautonomia. Ocular and bulbar symptoms may also occur, though respiratory failure is uncommon; we report the case of a 21-year-old woman diagnosed...

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Veröffentlicht in:Acta neurologica Belgica 2024-10
Hauptverfasser: Schön, Miguel, Campos, Catarina Falcão, Antunes, Ana Patrícia, Albuquerque, Luísa, Conceição, Isabel
Format: Artikel
Sprache:eng
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