Sensory ataxia

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Sensory ataxia is both a symptom and a sign in neurology. It is a form of ataxia (loss of coordination) caused not by cerebellar dysfunction but by loss of sensory input into the control of movement. [1]

Contents

Sensory ataxia is distinguished from cerebellar ataxia by the presence of near-normal coordination when the movement is visually observed by the patient, but marked worsening of coordination when the eyes are shut, indicating a positive Romberg's sign. [1]

Sensory ataxia also lacks the associated features of cerebellar ataxia such as pendular tendon reflexes, scanning dysarthria, nystagmus and broken pursuit eye movements.[ citation needed ]

Patients with sensory ataxia often demonstrate pseudoathetosis and Romberg's sign. They usually complain of loss of balance in the dark, typically when closing their eyes in the shower or removing clothing over the head.[ citation needed ]

Causes

Sensory ataxia can be a manifestation of sensory large fiber peripheral neuropathies and conditions causing dysfunction of the dorsal columns of the spinal cord due to a variety of disorders: infectious, auto-immune, metabolic, toxic, vascular and hereditary diseases. [2] [3] [4]

References

  1. 1 2 Zhang, Qing; Zhou, Xihui; Li, Yajun; Yang, Xiaodong; Abbasi, Qammer H. (2021). "Clinical Recognition of Sensory Ataxia and Cerebellar Ataxia". Frontiers in Human Neuroscience. 15: 639871. doi: 10.3389/fnhum.2021.639871 . ISSN   1662-5161. PMC   8046926 . PMID   33867960.
  2. Spinazzi M, Angelini C, Patrini C (May 2010). "Subacute sensory ataxia and optic neuropathy with thiamine deficiency". Nature Reviews Neurology. 6 (5): 288–93. doi:10.1038/nrneurol.2010.16. PMID   20308997. S2CID   12333200.
  3. Sghirlanzoni A, Pareyson D, Lauria G (June 2005). "Sensory neuron diseases". Lancet Neurol. 4 (6): 349–61. doi:10.1016/S1474-4422(05)70096-X. PMID   15907739. S2CID   35053543.
  4. Moeller JJ, Macaulay RJ, Valdmanis PN, Weston LE, Rouleau GA, Dupré N (September 2008). "Autosomal dominant sensory ataxia: a neuroaxonal dystrophy". Acta Neuropathol. 116 (3): 331–6. doi:10.1007/s00401-008-0362-6. PMID   18347805. S2CID   22881684.

Further reading