CC BY 4.0 · Arq Neuropsiquiatr 2023; 81(10): 934-936
DOI: 10.1055/s-0043-1775886
Historical Notes

Frontal ataxia: historical aspects and clinical definition

Ataxia frontal: aspectos históricos e definição clínica
1   Universidade Federal do Paraná, Hospital de Clínicas, Departamento de Medicina Interna, Serviço de Neurologia, Unidade de Distúrbios do Movimento, Curitiba PR, Brazil.
,
1   Universidade Federal do Paraná, Hospital de Clínicas, Departamento de Medicina Interna, Serviço de Neurologia, Unidade de Distúrbios do Movimento, Curitiba PR, Brazil.
,
1   Universidade Federal do Paraná, Hospital de Clínicas, Departamento de Medicina Interna, Serviço de Neurologia, Unidade de Distúrbios do Movimento, Curitiba PR, Brazil.
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1   Universidade Federal do Paraná, Hospital de Clínicas, Departamento de Medicina Interna, Serviço de Neurologia, Unidade de Distúrbios do Movimento, Curitiba PR, Brazil.
› Institutsangaben

Abstract

Frontal ataxia, originally described by Bruns, is characterized by the presence of signs of frontal lobe dysfunction, such as perseveration, paratonia, frontal release signs, cognitive changes, and urinary difficulty, associated with imbalance, slow gait, broad-based, the presence of postural instability and falls, retropulsion, and bradykinesia in the lower limbs. The goal of the present study is to recall the historical aspects of this condition, to draw attention to the importance of this clinical finding for the differential diagnosis of ataxias and to review the main semiological differences between primary ataxias (frontal, cerebellar, and sensory ataxia).

Resumo

A ataxia frontal, originalmente descrita por Bruns, caracteriza-se pela presença de sinais de disfunção do lobo frontal, como perseveração, paratonia, sinais de liberação frontal, alterações cognitivas e dificuldade urinária, associados a desequilíbrio, marcha lenta, base ampla, presença de instabilidade postural e quedas, retropulsão e bradicinesia em membros inferiores. O objetivo do presente trabalho é recordar os aspectos históricos desta condição, ressaltar a importância deste achado clínico para o diagnóstico diferencial das ataxias e revisar as principais diferenças semiológicas entre as ataxias primárias (ataxia frontal, cerebelar e sensitiva).

Authors' Contributions

PAAMB: conceptualization, data curation, writing – original draft, writing – review and editing; TEMN, BC: conceptualization, data curation; HAGT: conceptualization, data curation, formal analysis, supervision, validation, visualization, writing – original draft, writing – review and editing.




Publikationsverlauf

Eingereicht: 28. April 2023

Angenommen: 22. Juli 2023

Artikel online veröffentlicht:
29. Oktober 2023

© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)

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  • References

  • 1 Akbar U, Ashizawa T. Ataxia. Neurol Clin 2015; 33 (01) 225-248
  • 2 Garcin R. The ataxias. In: Vinken PJ, Bruyn GW. eds. Handbook of Clinical Neurology (volume 1). Amsterdam: North-Holland; 1969: 309-352
  • 3 Teive HAG, Munhoz RP, Ashizawa T. Inherited and sporadic ataxias. In: Albanese A, Jankovic J. (Eds). Hyperkinetic movement disorders. Differential diagnosis and treatment. Oxford, UK: Wiley-Blackwell; 2012: 279-295
  • 4 Teive HAG, Ashizawa T. Primary and secondary ataxias. Curr Opin Neurol 2015; 28 (04) 413-422
  • 5 Pandolfo M, Manto M. Cerebellar and afferent ataxias. Continuum (Minneap Minn) 2013; 19 (5 Movement Disorders): 1312-1343
  • 6 Chhetri SK, Gow D, Shaunak S, Varma A. Clinical assessment of the sensory ataxias; diagnostic algorithm with illustrative cases. Pract Neurol 2014; 14 (04) 242-251
  • 7 Gilman S. Gait disorders. In: Rowland LP. (Ed). Merrit's Neurology. Tenth Edition. Lippincott Williams & Wilkins; 2000: 45-49
  • 8 Pirker W, Katzenschlager R. Gait disorders in adults and the elderly : A clinical guide. Wien Klin Wochenschr 2017; 129 (3-4): 81-95
  • 9 Bruns L. Uber Störugen des Gleichgewichtes bei Stirnhirntumoren. Otsch Med Wochnschr 1892; 18: 138-140
  • 10 Anonymus. Ludwig Bruns. Whonamedit? - The dictionary of medical eponyms https://www.whonamedit.com (July, 07, 2023).
  • 11 Gerstmann J, Schilder P. Uber eine besondere Gangstorung bei Stirnhirner kranting. Wien Med Schr 1926; 76: 97-107
  • 12 Thompson PD, Marsden CD. Gait disorder of subcortical arteriosclerotic encephalopathy: Binswanger's disease. Mov Disord 1987; 2 (01) 1-8
  • 13 Thompson PD. Frontal lobe ataxia. Handb Clin Neurol 2012; 103: 619-622
  • 14 Terry JB, Rosenberg RN. Frontal lobe ataxia. Surg Neurol 1995; 44 (06) 583-588
  • 15 Marsden CD, Thompson P. Toward a nosology of gait disorders: Descriptive classification. In: Masdeau J, Sudarsky L, Wolfson L. Gait disorders of aging. Falls and therapeutic strategies. Lippincott-Raven Publishers; Philadelphia, USA: 1997: 135-146
  • 16 Nutt JG, Marsden CD, Thompson PD. Human walking and higher-level gait disorders, particularly in the elderly. Neurology 1993; 43 (02) 268-279
  • 17 Engelhardt E, Moreira DM, Laks J. Cerebrocerebellar system and Arnold's bundle - A tractographic study: preliminary results. Dement Neuropsychol 2010; 4 (04) 293-299