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Updated: Jun 14, 2026

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies
Published on: July 29, 2007
Acute motor and sensory axonal neuropathy in LEOPARD syndrome
Richard J Beukers1, Annemarie C M van Bellegem, Mariken Gruppen
1Department of Neurology, Academic Medical Center, University of Amsterdam, 1100 D Amsterdam, The Netherlands. r.j.beukers@amc.nl
Abstract:
A case of acute predominantly axonal motor and sensory neuropathy (AMSAN) is reported in a 16-year-old boy with LEOPARD syndrome (the acronym represents lentigines, ECG conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genitalia, retardation of growth, and sensorineural deafness). The presentation was atypical for acute motor and sensory axonal neuropathy, in that this patient had progression of symptoms of more than 4 weeks and there were signs of reinnervation in the acute phase. Treatment response to intravenous immunoglobulins was excellent. In patients with LEOPARD syndrome and acute neuropathies, treatment with intravenous immunoglobulins should be considered.
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