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Déjérine-Sottas disease |
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Déjérine-Sottas disease
[dezh′ərin sot′əz, -sotäz′] Etymology: Joseph J. Déjérine, French neurologist, 1849-1917; Jules Sottas, French neurologist, 1866-1943 a rare congenital spino-cerebellar disorder characterized by the development of palpable thickenings along peripheral nerves, degeneration of the peripheral nervous system, pain, paresthesia, ataxia, and diminished sensation and deep tendon reflexes. Diagnosis is made by a histologic examination of a peripheral nerve. There is no specific treatment. Also called progressive interstitial hypertrophic neuropathy. Want to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit the webmaster's page for free fun content. |
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