Evidence map›Paper›PMID 36187726›Full record

ReviewNeurology. Genetics2022

Overview of the Clinical Approach to Individuals With Cerebellar Ataxia and Neuropathy.

Leslie J Roberts, Michael McVeigh, Linda Seiderer, Ian H Harding, Louise A Corben, Martin Delatycki, David J Szmulewicz

Abstract readReview
In one paragraph

Review in Neurology. Genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
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  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Leslie J RobertsNeurophysiology Department (L.J.R.,L.S.), Department of Neurology & Neurological Research, St Vincent's Hospital; Department of Medicine (L.J.R., L.S.), the University of Melbourne; Ballance Disorders and Ataxia Service (L.J.R., M.M., D.J.S.), Eye and Ear Hospital; Department of Neuroscience (I.H.H., L.A.C.), Central Clinical School, Monash University; Monash Biomedical Imaging (I.H.H., L.A.C.), Monash University; Bruce Lefroy Centre (L.A.C.), Murdoch Children's Research Institute; 7Department of Paediatrics, Melbourne University; Turner Institute for Brain and Mental Health, Monash University; Victorian Clinical Genetics Services (M.D.), Murdoch Children's Reseach Institute; and The Florey Institute of Neuroscience and Mental Health (D.J.S.), the University of Melbourne, Australia.
Michael McVeighNeurophysiology Department (L.J.R.,L.S.), Department of Neurology & Neurological Research, St Vincent's Hospital; Department of Medicine (L.J.R., L.S.), the University of Melbourne; Ballance Disorders and Ataxia Service (L.J.R., M.M., D.J.S.), Eye and Ear Hospital; Department of Neuroscience (I.H.H., L.A.C.), Central Clinical School, Monash University; Monash Biomedical Imaging (I.H.H., L.A.C.), Monash University; Bruce Lefroy Centre (L.A.C.), Murdoch Children's Research Institute; 7Department of Paediatrics, Melbourne University; Turner Institute for Brain and Mental Health, Monash University; Victorian Clinical Genetics Services (M.D.), Murdoch Children's Reseach Institute; and The Florey Institute of Neuroscience and Mental Health (D.J.S.), the University of Melbourne, Australia.
Linda SeidererNeurophysiology Department (L.J.R.,L.S.), Department of Neurology & Neurological Research, St Vincent's Hospital; Department of Medicine (L.J.R., L.S.), the University of Melbourne; Ballance Disorders and Ataxia Service (L.J.R., M.M., D.J.S.), Eye and Ear Hospital; Department of Neuroscience (I.H.H., L.A.C.), Central Clinical School, Monash University; Monash Biomedical Imaging (I.H.H., L.A.C.), Monash University; Bruce Lefroy Centre (L.A.C.), Murdoch Children's Research Institute; 7Department of Paediatrics, Melbourne University; Turner Institute for Brain and Mental Health, Monash University; Victorian Clinical Genetics Services (M.D.), Murdoch Children's Reseach Institute; and The Florey Institute of Neuroscience and Mental Health (D.J.S.), the University of Melbourne, Australia.
Ian H HardingNeurophysiology Department (L.J.R.,L.S.), Department of Neurology & Neurological Research, St Vincent's Hospital; Department of Medicine (L.J.R., L.S.), the University of Melbourne; Ballance Disorders and Ataxia Service (L.J.R., M.M., D.J.S.), Eye and Ear Hospital; Department of Neuroscience (I.H.H., L.A.C.), Central Clinical School, Monash University; Monash Biomedical Imaging (I.H.H., L.A.C.), Monash University; Bruce Lefroy Centre (L.A.C.), Murdoch Children's Research Institute; 7Department of Paediatrics, Melbourne University; Turner Institute for Brain and Mental Health, Monash University; Victorian Clinical Genetics Services (M.D.), Murdoch Children's Reseach Institute; and The Florey Institute of Neuroscience and Mental Health (D.J.S.), the University of Melbourne, Australia.
Louise A CorbenNeurophysiology Department (L.J.R.,L.S.), Department of Neurology & Neurological Research, St Vincent's Hospital; Department of Medicine (L.J.R., L.S.), the University of Melbourne; Ballance Disorders and Ataxia Service (L.J.R., M.M., D.J.S.), Eye and Ear Hospital; Department of Neuroscience (I.H.H., L.A.C.), Central Clinical School, Monash University; Monash Biomedical Imaging (I.H.H., L.A.C.), Monash University; Bruce Lefroy Centre (L.A.C.), Murdoch Children's Research Institute; 7Department of Paediatrics, Melbourne University; Turner Institute for Brain and Mental Health, Monash University; Victorian Clinical Genetics Services (M.D.), Murdoch Children's Reseach Institute; and The Florey Institute of Neuroscience and Mental Health (D.J.S.), the University of Melbourne, Australia.ORCID https://orcid.org/0000-0001-8767-4582
Martin DelatyckiNeurophysiology Department (L.J.R.,L.S.), Department of Neurology & Neurological Research, St Vincent's Hospital; Department of Medicine (L.J.R., L.S.), the University of Melbourne; Ballance Disorders and Ataxia Service (L.J.R., M.M., D.J.S.), Eye and Ear Hospital; Department of Neuroscience (I.H.H., L.A.C.), Central Clinical School, Monash University; Monash Biomedical Imaging (I.H.H., L.A.C.), Monash University; Bruce Lefroy Centre (L.A.C.), Murdoch Children's Research Institute; 7Department of Paediatrics, Melbourne University; Turner Institute for Brain and Mental Health, Monash University; Victorian Clinical Genetics Services (M.D.), Murdoch Children's Reseach Institute; and The Florey Institute of Neuroscience and Mental Health (D.J.S.), the University of Melbourne, Australia.
David J SzmulewiczNeurophysiology Department (L.J.R.,L.S.), Department of Neurology & Neurological Research, St Vincent's Hospital; Department of Medicine (L.J.R., L.S.), the University of Melbourne; Ballance Disorders and Ataxia Service (L.J.R., M.M., D.J.S.), Eye and Ear Hospital; Department of Neuroscience (I.H.H., L.A.C.), Central Clinical School, Monash University; Monash Biomedical Imaging (I.H.H., L.A.C.), Monash University; Bruce Lefroy Centre (L.A.C.), Murdoch Children's Research Institute; 7Department of Paediatrics, Melbourne University; Turner Institute for Brain and Mental Health, Monash University; Victorian Clinical Genetics Services (M.D.), Murdoch Children's Reseach Institute; and The Florey Institute of Neuroscience and Mental Health (D.J.S.), the University of Melbourne, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasingly, cerebellar syndromes are recognized as affecting multiple systems. Extracerebellar features include peripheral neuropathies affecting proprioception; cranial neuropathies such as auditory and vestibular; and neuronopathies, for example, dorsal root and vestibular. The presence of such features, which in and of themselves may cause ataxia, likely contribute to key disabilities such as gait instability and falls. Based on the evolving available literature and experience, we outline a clinical approach to the diagnosis of adult-onset ataxia where a combination of cerebellar and peripheral or cranial nerve pathology exists. Objective diagnostic modalities including electrophysiology, oculomotor, and vestibular function testing are invaluable in accurately defining an individual's phenotype. Advances in MRI techniques have led to an increased recognition of disease-specific patterns of cerebellar pathology, including those conditions where neuronopathies may be involved. Depending on availability, a stepwise approach to genetic testing is suggested. This is guided by factors such as pattern of inheritance and age at disease onset, and genetic testing may range from specific genetic panels through to whole-exome and whole-genome sequencing. Management is best performed with the involvement of a multidisciplinary team, aiming at minimization of complications such as falls and aspiration pneumonia and maximizing functional status.

Identifiers

PMID36187726
PMCPMC9520343

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.