Literature DB >> 12628066

Gait and Balance Dysfunction in Adults.

Salil Manek1, Mark F. Lew.   

Abstract

Determining the precise cause of gait dysfunction in adults is often difficult because of the multifactorial nature of the disorder. Additionally, elderly patients have other comorbidities that further complicate their diagnosis. A proper history and physical examination, however, often allow the clinician to arrive at the correct diagnosis. Once a diagnosis is reached, appropriate therapeutic decisions can be made. Patients presenting with Parkinsonism need a thorough evaluation to rule out potentially reversible conditions, such as normal pressure hydrocephalus. Patients with idiopathic Parkinson's disease usually develop gait difficulty and freezing episodes late in the course of the illness. Another important cause of gait disturbance in adults is the cerebellar ataxias. Among the sporadic forms, gluten sensitivity is an important consideration. Identification of this entity is important, because the disease process can be halted with a gluten-free diet. Another group is the paraneoplastic ataxias, which can often be diagnosed in the proper clinical setting. Most of the adult-onset hereditary ataxias are autosomal dominant conditions. Except for the episodic ataxias, treatment of these conditions has been disappointing. Mixed results have been obtained with the use of amantadine, buspirone, and 5-hydroxytryptophan. Physical therapy plays an important role in the gait rehabilitation of these patients. Over the past several years, researchers have developed a greater understanding of motor control and how it relates to freezing. Clinicians can now train patients to use external cues to overcome their motor blocks. Another important advance has been the development of subthalamic nucleus deep brain stimulation in the treatment of patients with troublesome peak dose dyskinesia and other motor fluctuations. Subthalamic nucleus deep brain stimulation should be considered when best medical treatment fails. Cortical myoclonus can be treated with levetiracetam, which has US Food and Drug Administration approval as an antiepileptic agent. It has been quite effective in the treatment of myoclonus and should be considered when other medications fail.

Entities:  

Year:  2003        PMID: 12628066     DOI: 10.1007/s11940-003-0008-x

Source DB:  PubMed          Journal:  Curr Treat Options Neurol        ISSN: 1092-8480            Impact factor:   3.598


  53 in total

1.  Effect of subthalamic nucleus stimulation on levodopa-induced dyskinesia in Parkinson's disease.

Authors:  V Fraix; P Pollak; N Van Blercom; J Xie; P Krack; A Koudsie; A L Benabid
Journal:  Neurology       Date:  2000-12-26       Impact factor: 9.910

2.  Riluzole and olanzapine in Huntington's disease.

Authors:  Raphael M Bonelli; G Niederwieser; J Diez; P Költringer
Journal:  Eur J Neurol       Date:  2002-03       Impact factor: 6.089

3.  Surgery for movement disorders.

Authors:  Ralph Gregory
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-03       Impact factor: 10.154

4.  Clozapine versus placebo in Huntington's disease: a double blind randomised comparative study.

Authors:  J P van Vugt; S Siesling; M Vergeer; E A van der Velde; R A Roos
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-07       Impact factor: 10.154

Review 5.  Myoclonus.

Authors:  J N Caviness
Journal:  Mayo Clin Proc       Date:  1996-07       Impact factor: 7.616

6.  The treatment of spinocerebellar ataxias: facts and hypotheses.

Authors:  M I Botez; T Botez-Marquard; P Mayer; L Marchand; R Lalonde; T A Reader
Journal:  Med Hypotheses       Date:  1998-11       Impact factor: 1.538

7.  Bilateral human fetal striatal transplantation in Huntington's disease.

Authors:  R A Hauser; S Furtado; C R Cimino; H Delgado; S Eichler; S Schwartz; D Scott; G M Nauert; E Soety; V Sossi; D A Holt; P R Sanberg; A J Stoessl; T B Freeman
Journal:  Neurology       Date:  2002-03-12       Impact factor: 9.910

8.  Gluten sensitivity in sporadic and hereditary cerebellar ataxia.

Authors:  K O Bushara; S U Goebel; H Shill; L G Goldfarb; M Hallett
Journal:  Ann Neurol       Date:  2001-04       Impact factor: 10.422

9.  Movement disorders in people with Parkinson disease: a model for physical therapy.

Authors:  M E Morris
Journal:  Phys Ther       Date:  2000-06

10.  Suppression of post-hypoxic and post-encephalitic myoclonus with levetiracetam.

Authors:  G L Krauss; A Bergin; R E Kramer; Y W Cho; S G Reich
Journal:  Neurology       Date:  2001-02-13       Impact factor: 9.910

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  1 in total

1.  Deep Brain Stimulation Surgery for Parkinson Disease Coexisting With Communicating Hydrocephalus: A Case Report.

Authors:  Carlos Guevara; Jose de Grazia; Pedro Vazquez; Pablo Baabor; Cristián Garrido; Melissa Martinez; Jaime Fuentes; Fabian Piedimonte; Marcos Baabor
Journal:  Front Neurol       Date:  2018-11-23       Impact factor: 4.003

  1 in total

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