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The syndrome of inappropriate secretion of antidiuretic hormone (SIADH) is observed in up to 26% of patients with Guillain–Barre syndrome (GBS), usually at the time of maximal motor deficit.1 SIADH is characterized by fluid retention leading to decreased sodium concentration and serum osmolality. We report a case of GBS with SIADH clearly preceding the evolution of paresis, paresthesia, and areflexia. A 38-year-old woman was referred to our hospital because of severe headaches and mild confusion that had developed 5 days after a gastrointestinal infection. Neurologic examination on admission was unremarkable except for a marked weariness and reduced vibration sense at the toes (3/8). The latter finding was related to Type I diabetes mellitus diagnosed 20 years before. CT and angiogram (to exclude dural sinus thrombosis) were normal. CSF revealed 8 cells/μL, mostly lymphocytes, …
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Hoffmann et al. (1999) studied this question.
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