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Can loss of muscle spindle afferents explain the ataxic gait in Riley–Day syndrome?

The Riley–Day syndrome is the most common of the hereditary sensory and autonomic neuropathies (Type III). Among the well-recognized clinical features are reduced pain and temperature sensation, absent deep tendon reflexes and a progressively ataxic gait. To explain the latter we tested the hypothes...

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Autori principali: Macefield, Vaughan G., Norcliffe-Kaufmann, Lucy, Gutiérrez, Joel, Axelrod, Felicia B., Kaufmann, Horacio
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2011
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3212710/
https://ncbi.nlm.nih.gov/pubmed/22075519
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awr168
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