Dorsal root ganglionopathy is responsible for the sensory impairment in CANVAS

被引:95
作者
Szmulewicz, David J. [1 ]
McLean, Catriona A. [2 ]
Rodriguez, Michael L.
Chancellor, Andrew M. [3 ]
Mossman, Stuart [4 ]
Lamont, Duncan [5 ]
Roberts, Leslie [6 ]
Storey, Elsdon [7 ]
Halmagyi, G. Michael [8 ]
机构
[1] Univ Melbourne, Royal Victorian Eye & Ear Hosp, Melbourne, Vic, Australia
[2] Alfred Hosp, Dept Anat Pathol, Melbourne, Vic, Australia
[3] Tauranga Hosp, Dept Med, Wellington, New Zealand
[4] Capital Coast Hlth, Dept Neurol, Wellington, New Zealand
[5] Waikato Hosp, Hamilton, Waikato, New Zealand
[6] St Vincents Hosp, Dept Neurosci, Melbourne, Vic, Australia
[7] Monash Univ, Dept Neurosci, Melbourne, Vic 3004, Australia
[8] Royal Prince Alfred Hosp, Dept Neurol, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
VESTIBULAR AREFLEXIA SYNDROME; SPINOCEREBELLAR ATAXIA; CEREBELLAR-ATAXIA; FRIEDREICHS-ATAXIA; NEUROPATHY; FEATURES; ATROPHY;
D O I
10.1212/WNL.0000000000000352
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective:To elucidate the neuropathology in cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (CANVAS), a novel cerebellar ataxia comprised of the triad of cerebellar impairment, bilateral vestibular hypofunction, and a peripheral sensory deficit.Method:Brain and spinal neuropathology in 2 patients with CANVAS, together with brain and otopathology in another patient with CANVAS, were examined postmortem.Results:Spinal cord pathology demonstrated a marked dorsal root ganglionopathy with secondary tract degeneration. Cerebellar pathology showed loss of Purkinje cells, predominantly in the vermis.Conclusion:The likely underlying sensory pathology in CANVAS is loss of neurons from the dorsal root and V, VII, and VIII cranial nerve gangliain other words, it is a neuronopathy rather than a neuropathy. Clinically, CANVAS is a differential diagnosis for both spinocerebellar ataxia type 3 (or Machado-Joseph disease) and Friedreich ataxia. In addition, there are 6 sets of sibling pairs, implying that CANVAS is likely to be a late-onset recessive or autosomal dominant with reduced penetrance disorder, and identification of the culprit gene is currently a target of investigation.
引用
收藏
页码:1410 / 1415
页数:6
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