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1.
Int J Rehabil Res ; 31(4): 342-6, 2008 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19008684

RESUMO

The objective of this study was to investigate the long-term efficacy of inpatient rehabilitation using sleeping neck support in patients suffering from chronic cervicobrachialgia. A prospective, randomized clinical trial with a 12-month follow-up was done. A total of 149 patients suffering from chronic cervicobrachialgia received a 4-week inpatient rehabilitation programme. The patients were randomly divided into two groups. The patients in one group were given a special neck pillow to use during and after the rehabilitative treatment (n=76); the patients in the other group were not given the pillow (n=73). Two weeks before, during, and after (3, 6, 9, and 12 months) the 4-week treatment period, the patients completed a questionnaire dealing with the intensity of their cervicobrachial complaints (pain intensity, muscular tension, paraesthesia, and sleep disorders caused by pain or paraesthesia). During the inpatient treatment period, no significant differences were detected between the groups; however, 1-12 months after discharge, the group with sleeping neck support showed a significantly (P<0.05) smaller increase in the intensity of cervical spine pain. Sleep disturbances caused by pain were also reduced significantly (P<0.001 after 3 months, respectively, P<0.05 after 12 months). Inpatient rehabilitative treatment has sustained effects in patients suffering from chronic cervicobrachialgia, particularly when a sleeping neck support is added.


Assuntos
Roupas de Cama, Mesa e Banho , Neurite do Plexo Braquial/reabilitação , Neurite do Plexo Braquial/classificação , Doença Crônica , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Modalidades de Fisioterapia , Centros de Reabilitação , Índice de Gravidade de Doença , Sono , Inquéritos e Questionários
2.
Neurology ; 44(12): 2253-7, 1994 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-7991108

RESUMO

Hereditary neuralgic amyotrophy with predilection for the brachial plexus (HNA) and hereditary neuropathy with liability to pressure palsies (HNPP) are autosomal dominant disorders associated with episodic, recurrent brachial neuropathies. HNPP is associated with a deletion or abnormal structure of the PMP22 gene on chromosome 17p11.2-12. The genetic locus for HNA is unknown. To address the possibility that HNPP and HNA might be identical disorders or allelic variations at the same locus, we investigated three HNA pedigrees with markers from the HNPP region. We did not find the 17p11.2-12 deletion associated with HNPP, nor an abnormality in PMP22 structure with HNA. This analysis provides genetic evidence, in addition to that suggested by the clinical, electrophysiologic, and pathologic differences, that HNA and HNPP are distinct disorders.


Assuntos
Neurite do Plexo Braquial/genética , Cromossomos Humanos Par 17 , Proteínas da Mielina/genética , Doenças do Sistema Nervoso Periférico/genética , Adolescente , Adulto , Idade de Início , Neurite do Plexo Braquial/classificação , Criança , Pré-Escolar , Mapeamento Cromossômico , Feminino , Marcadores Genéticos , Humanos , Masculino , Pessoa de Meia-Idade , Linhagem , Doenças do Sistema Nervoso Periférico/classificação , Recombinação Genética
3.
Neurology ; 44(12): 2250-2, 1994 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-7991107

RESUMO

Hereditary neuralgic amyotrophy (HNA) is an autosomal disease characterized by painful episodes of brachial palsy. The presence of tomacula in some patients suggested that HNA might be genetically related to hereditary neuropathy with liability to pressure palsies (HNPP), caused by point mutations in the PMP22 gene or deletion of the region containing this gene. In a clinical, electrophysiologic, and molecular study of two families with HNA, we show that the PMP22 gene is not deleted, duplicated, or mutated in HNA and that the disease is not linked to any other gene in the HNPP deleted region. We conclude that HNA and HNPP are distinct genetic entities.


Assuntos
Neurite do Plexo Braquial/fisiopatologia , Proteínas da Mielina/genética , Doenças do Sistema Nervoso Periférico/fisiopatologia , Adolescente , Adulto , Neurite do Plexo Braquial/classificação , Neurite do Plexo Braquial/genética , Criança , Cromossomos Humanos Par 17 , Feminino , Deleção de Genes , Triagem de Portadores Genéticos , Ligação Genética , Genótipo , Humanos , Masculino , Linhagem , Doenças do Sistema Nervoso Periférico/classificação , Doenças do Sistema Nervoso Periférico/genética , Mutação Puntual , Polimorfismo de Fragmento de Restrição , Pressão
5.
J Hum Ergol (Tokyo) ; 8(1): 39-45, 1979 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-398864

RESUMO

Recent rapid development of mechanization and automatization in many industries in Japan have increased simple and repetitive tasks that have resulted in some new types of occupational health hazards, in particular among young female workers. One of them is occupational cervicobrachial disorder, the concept of which was established by the committee organized by the Japan Association of Industrial Health in 1972. The committee demonstrated that the disorder resulted from repetitive upper limb manipulation in punching and operating various kinds of business machines, and concluded that the disorder was closely related to chronic fatigue in the shoulders, neck, lower back and other parts of the body. In 1975 a study team was organized with a grant from the Ministry of Education. The team was divided into four working groups. Topics of these groups were 1) etiology of the disorder, 2) natural history of the disorder in various kinds of jobs, 3) mass examination techniques for the disorder, and 4) a health care system to be provided for the workers. The persent report summarizes the results of group discussions with a view to indicating the current problems of occupational cervicobrachial disorder and the necessary future steps for its care treatment and prevention.


Assuntos
Neurite do Plexo Braquial/etiologia , Doenças Profissionais/prevenção & controle , Neurite do Plexo Braquial/classificação , Humanos , Japão
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