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Published on: November 4, 2017
Progressive encephalomyelitis with rigidity and myoclonus (PERM)
Neil Grech1,2, John Paul Caruana Galizia3, Adrian Pace4
1Department of Medicine, Mater Dei Hospital, Msida, Malta neil.b.grech@gov.mt.
Abstract:
Progressive encephalomyelitis with rigidity and myoclonus (PERM) is a subtype of stiff-person syndrome (formerly stiff-man syndrome). It is rare and disabling, and characterised by brainstem symptoms, muscle stiffness, breathing issues and autonomic dysfunction. We describe a 65-year-old man who presented with odynophagia together with tongue and neck swelling, followed by multiple cranial nerve palsies culminating in bilateral vocal cord paralysis with acute stridor. He subsequently developed progressive generalised hypertonia and painful limb spasms. Serum antiglycine receptor antibody was strongly positive, but antiglutamic acid decarboxylase and other antibodies relating to stiff-person syndrome were negative. We diagnosed PERM and gave intravenous corticosteroids and immunoglobulins without benefit; however, following plasma exchange he has made a sustained improvement.
Insights
Progressive encephalomyelitis with rigidity and myoclonus (PERM) is a rare neurological disorder. Plasma exchange therapy showed sustained improvement in a patient with anti-glycine receptor antibody-positive PERM.
Area of Science:
- Neurology
- Immunology
Background:
- Progressive encephalomyelitis with rigidity and myoclonus (PERM) is a rare, disabling subtype of stiff-person syndrome.
- PERM is characterized by brainstem symptoms, muscle stiffness, respiratory compromise, and autonomic dysfunction.
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