Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará

Detalhes bibliográficos
Ano de defesa: 2021
Autor(a) principal: Sobrinho, Jéssica Queiroz de Sousa
Orientador(a): Gondim, Francisco de Assis Aquino
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Não Informado pela instituição
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://www.repositorio.ufc.br/handle/riufc/60405
Resumo: Wilson's disease (DW) is a rare autosomal recessive disorder, not linked to sex, due to a mutation in the ATP7B gene, which generates changes in copper metabolism. It is a systemic disease characterized by hepatic, neurological and musculoskeletal disorders. Studies carried out with people affected by this disease in Brazil involved only the population of the south and southeast of the country. The aim of this study was to describe the central and peripheral neurological disorders in patients with Wilson's disease in the state of Ceará. 14 patients with a conclusive diagnosis of DW were recruited, accompanied by a neurologist at the Hospital Universitário Walter Cantídio (HUWC). Patients had their medical records reviewed; performed anamnesis, neurological evaluation, skin wrinkle test and answered the Quality of Life Determination (DEFU) questionnaires, Barthel Index and the Compound Score of Autonomic Symptoms (COMPASS 31). The mean age at the time of the patient survey was 39.4+ 2.61 years (25 to 53 years). All patients had neurological changes. Among these 8 had a positive family history of DW involving siblings, cousins and nephews, 10 patients had consanguineous parents and 6 lived in inland regions. The average age for the conclusive diagnosis of DW was 24.5 years ± 1.40 years (from 13 to 34 years). The most common neurological symptoms were: tremor, dysphagia, dysarthria, change in gait, stiffness, drooling, speech disorders and bradykinesia. The most common neurological signs were: tremor, cogwheel signal, Kayser Fleisher rings and Babinski signal. The most widely used pharmacological treatment was penicillamine. The most reported psychiatric symptom was depression. Among the evaluated patients, 71.4% (10) presented some symptom of autonomic dysfunction, of which 57% (8) obtained an abnormal result in the skin wrinkle test by immersing the hand in water. Among the neurological characteristics presented by the patients in this study, the involvement of sensitive and autonomic peripheral nerve fibers from the skin wrinkle test stands out. Our study proves the presence of peripheral neuropathy in 50% of patients affected with DW, as well as the correlation of this dysfunction with the presence of autonomic disorders.
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spelling Sobrinho, Jéssica Queiroz de SousaGondim, Francisco de Assis Aquino2021-09-13T11:44:24Z2021-09-13T11:44:24Z2021-06-18SOBRINHO, J. Q. S. Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará. 2021. 175 f. Dissertação (Mestrado em Ciências Morfofuncionais) - Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, 2021.http://www.repositorio.ufc.br/handle/riufc/60405Wilson's disease (DW) is a rare autosomal recessive disorder, not linked to sex, due to a mutation in the ATP7B gene, which generates changes in copper metabolism. It is a systemic disease characterized by hepatic, neurological and musculoskeletal disorders. Studies carried out with people affected by this disease in Brazil involved only the population of the south and southeast of the country. The aim of this study was to describe the central and peripheral neurological disorders in patients with Wilson's disease in the state of Ceará. 14 patients with a conclusive diagnosis of DW were recruited, accompanied by a neurologist at the Hospital Universitário Walter Cantídio (HUWC). Patients had their medical records reviewed; performed anamnesis, neurological evaluation, skin wrinkle test and answered the Quality of Life Determination (DEFU) questionnaires, Barthel Index and the Compound Score of Autonomic Symptoms (COMPASS 31). The mean age at the time of the patient survey was 39.4+ 2.61 years (25 to 53 years). All patients had neurological changes. Among these 8 had a positive family history of DW involving siblings, cousins and nephews, 10 patients had consanguineous parents and 6 lived in inland regions. The average age for the conclusive diagnosis of DW was 24.5 years ± 1.40 years (from 13 to 34 years). The most common neurological symptoms were: tremor, dysphagia, dysarthria, change in gait, stiffness, drooling, speech disorders and bradykinesia. The most common neurological signs were: tremor, cogwheel signal, Kayser Fleisher rings and Babinski signal. The most widely used pharmacological treatment was penicillamine. The most reported psychiatric symptom was depression. Among the evaluated patients, 71.4% (10) presented some symptom of autonomic dysfunction, of which 57% (8) obtained an abnormal result in the skin wrinkle test by immersing the hand in water. Among the neurological characteristics presented by the patients in this study, the involvement of sensitive and autonomic peripheral nerve fibers from the skin wrinkle test stands out. Our study proves the presence of peripheral neuropathy in 50% of patients affected with DW, as well as the correlation of this dysfunction with the presence of autonomic disorders.A Doença de Wilson (DW) é um distúrbio autossômico recessivo raro, não ligado ao sexo, decorrente de mutação no gene ATP7B, que gera alteração no metabolismo do cobre. Trata-se de uma doença sistêmica e caracterizada por comprometimentos hepáticos, neurológicos e osteomusculares. Os estudos realizados com pessoas acometidas por essa doença no Brasil envolveram apenas a população do sul e sudeste do país. O objetivo desse estudo consistiu em descrever as alterações neurológicas centrais e periféricas em pacientes com doença de Wilson do estado do Ceará. Foram recrutados 14 pacientes com diagnóstico conclusivo de DW acompanhados por neurologista no Hospital Universitário Walter Cantídio (HUWC). Os pacientes tiveram seus prontuários revisados; realizaram anamnese, avaliação neurológica, teste de enrugamento cutâneo e responderam aos questionários de Determinação de Qualidade de Vida (DEFU), Índice de Barthel e a Pontuação Composta de Sintomas Autonômicos (COMPASS 31).A idade média até o momento da pesquisa dos pacientes foi de 39,4+2,61 anos (25 a 53 anos). Todos os pacientes apresentaram alterações neurológicas. Entre estes 8 apresentaram histórico familiar positivo de DW envolvendo irmãos, primos e sobrinho, 10 pacientes tinham pais consanguíneos e 6 residiam em regiões interioranas. A média de idade para o diagnóstico conclusivo de DW foi de 24,5 anos±1,40 anos (de 13 a 34 anos). Os sintomas neurológicos mais comuns foram: tremor, disfagia, disartria, alteração da marcha, rigidez, sialorreia, alteração da fala e bradicinesia. Os sinais neurológicos mais comuns foram: tremor, sinal de roda denteada, anéis de Kayser Fleisher e sinal de Babinski. O tratamento farmacológico mais utilizado foi a penicilamina. O sintoma psiquiátrico mais relatado foi quadro depressivo. Dentre os pacientes avaliados 71,4% (10) apresentaram algum sintoma de disfunção autonômica, desses 57% (8) obtiveram resultado anormal no teste de enrugamento cutâneo por imersão da mão na água. Dentre as características neurológicas apresentadas pelos pacientes desse estudo, destaca-se o acometimento das fibras nervosas periféricas sensitivas e autonômicas a partir do teste de enrugamento cutâneo. Nosso estudo comprova a presença de neuropatia periférica em 50% dos pacientes acometidos com DW, assim como a correlação dessa disfunção com a presença de distúrbios autonômicos.Doença de WilsonNeuropatia de Pequenas FibrasSistema NervosoEstudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Cearáinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisporreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccessORIGINAL2021_dis_jqssobrinho.pdf2021_dis_jqssobrinho.pdfapplication/pdf3152509http://repositorio.ufc.br/bitstream/riufc/60405/6/2021_dis_jqssobrinho.pdf6a05123fef1ac62416b9440c61b97e83MD56LICENSElicense.txtlicense.txttext/plain; charset=utf-81748http://repositorio.ufc.br/bitstream/riufc/60405/7/license.txt8a4605be74aa9ea9d79846c1fba20a33MD57riufc/604052021-09-13 08:47:16.846oai:repositorio.ufc.br:riufc/60405Tk9URTogUExBQ0UgWU9VUiBPV04gTElDRU5TRSBIRVJFClRoaXMgc2FtcGxlIGxpY2Vuc2UgaXMgcHJvdmlkZWQgZm9yIGluZm9ybWF0aW9uYWwgcHVycG9zZXMgb25seS4KCk5PTi1FWENMVVNJVkUgRElTVFJJQlVUSU9OIExJQ0VOU0UKCkJ5IHNpZ25pbmcgYW5kIHN1Ym1pdHRpbmcgdGhpcyBsaWNlbnNlLCB5b3UgKHRoZSBhdXRob3Iocykgb3IgY29weXJpZ2h0Cm93bmVyKSBncmFudHMgdG8gRFNwYWNlIFVuaXZlcnNpdHkgKERTVSkgdGhlIG5vbi1leGNsdXNpdmUgcmlnaHQgdG8gcmVwcm9kdWNlLAp0cmFuc2xhdGUgKGFzIGRlZmluZWQgYmVsb3cpLCBhbmQvb3IgZGlzdHJpYnV0ZSB5b3VyIHN1Ym1pc3Npb24gKGluY2x1ZGluZwp0aGUgYWJzdHJhY3QpIHdvcmxkd2lkZSBpbiBwcmludCBhbmQgZWxlY3Ryb25pYyBmb3JtYXQgYW5kIGluIGFueSBtZWRpdW0sCmluY2x1ZGluZyBidXQgbm90IGxpbWl0ZWQgdG8gYXVkaW8gb3IgdmlkZW8uCgpZb3UgYWdyZWUgdGhhdCBEU1UgbWF5LCB3aXRob3V0IGNoYW5naW5nIHRoZSBjb250ZW50LCB0cmFuc2xhdGUgdGhlCnN1Ym1pc3Npb24gdG8gYW55IG1lZGl1bSBvciBmb3JtYXQgZm9yIHRoZSBwdXJwb3NlIG9mIHByZXNlcnZhdGlvbi4KCllvdSBhbHNvIGFncmVlIHRoYXQgRFNVIG1heSBrZWVwIG1vcmUgdGhhbiBvbmUgY29weSBvZiB0aGlzIHN1Ym1pc3Npb24gZm9yCnB1cnBvc2VzIG9mIHNlY3VyaXR5LCBiYWNrLXVwIGFuZCBwcmVzZXJ2YXRpb24uCgpZb3UgcmVwcmVzZW50IHRoYXQgdGhlIHN1Ym1pc3Npb24gaXMgeW91ciBvcmlnaW5hbCB3b3JrLCBhbmQgdGhhdCB5b3UgaGF2ZQp0aGUgcmlnaHQgdG8gZ3JhbnQgdGhlIHJpZ2h0cyBjb250YWluZWQgaW4gdGhpcyBsaWNlbnNlLiBZb3UgYWxzbyByZXByZXNlbnQKdGhhdCB5b3VyIHN1Ym1pc3Npb24gZG9lcyBub3QsIHRvIHRoZSBiZXN0IG9mIHlvdXIga25vd2xlZGdlLCBpbmZyaW5nZSB1cG9uCmFueW9uZSdzIGNvcHlyaWdodC4KCklmIHRoZSBzdWJtaXNzaW9uIGNvbnRhaW5zIG1hdGVyaWFsIGZvciB3aGljaCB5b3UgZG8gbm90IGhvbGQgY29weXJpZ2h0LAp5b3UgcmVwcmVzZW50IHRoYXQgeW91IGhhdmUgb2J0YWluZWQgdGhlIHVucmVzdHJpY3RlZCBwZXJtaXNzaW9uIG9mIHRoZQpjb3B5cmlnaHQgb3duZXIgdG8gZ3JhbnQgRFNVIHRoZSByaWdodHMgcmVxdWlyZWQgYnkgdGhpcyBsaWNlbnNlLCBhbmQgdGhhdApzdWNoIHRoaXJkLXBhcnR5IG93bmVkIG1hdGVyaWFsIGlzIGNsZWFybHkgaWRlbnRpZmllZCBhbmQgYWNrbm93bGVkZ2VkCndpdGhpbiB0aGUgdGV4dCBvciBjb250ZW50IG9mIHRoZSBzdWJtaXNzaW9uLgoKSUYgVEhFIFNVQk1JU1NJT04gSVMgQkFTRUQgVVBPTiBXT1JLIFRIQVQgSEFTIEJFRU4gU1BPTlNPUkVEIE9SIFNVUFBPUlRFRApCWSBBTiBBR0VOQ1kgT1IgT1JHQU5JWkFUSU9OIE9USEVSIFRIQU4gRFNVLCBZT1UgUkVQUkVTRU5UIFRIQVQgWU9VIEhBVkUKRlVMRklMTEVEIEFOWSBSSUdIVCBPRiBSRVZJRVcgT1IgT1RIRVIgT0JMSUdBVElPTlMgUkVRVUlSRUQgQlkgU1VDSApDT05UUkFDVCBPUiBBR1JFRU1FTlQuCgpEU1Ugd2lsbCBjbGVhcmx5IGlkZW50aWZ5IHlvdXIgbmFtZShzKSBhcyB0aGUgYXV0aG9yKHMpIG9yIG93bmVyKHMpIG9mIHRoZQpzdWJtaXNzaW9uLCBhbmQgd2lsbCBub3QgbWFrZSBhbnkgYWx0ZXJhdGlvbiwgb3RoZXIgdGhhbiBhcyBhbGxvd2VkIGJ5IHRoaXMKbGljZW5zZSwgdG8geW91ciBzdWJtaXNzaW9uLgo=Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2021-09-13T11:47:16Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.pt_BR.fl_str_mv Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará
title Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará
spellingShingle Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará
Sobrinho, Jéssica Queiroz de Sousa
Doença de Wilson
Neuropatia de Pequenas Fibras
Sistema Nervoso
title_short Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará
title_full Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará
title_fullStr Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará
title_full_unstemmed Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará
title_sort Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará
author Sobrinho, Jéssica Queiroz de Sousa
author_facet Sobrinho, Jéssica Queiroz de Sousa
author_role author
dc.contributor.author.fl_str_mv Sobrinho, Jéssica Queiroz de Sousa
dc.contributor.advisor1.fl_str_mv Gondim, Francisco de Assis Aquino
contributor_str_mv Gondim, Francisco de Assis Aquino
dc.subject.por.fl_str_mv Doença de Wilson
Neuropatia de Pequenas Fibras
Sistema Nervoso
topic Doença de Wilson
Neuropatia de Pequenas Fibras
Sistema Nervoso
description Wilson's disease (DW) is a rare autosomal recessive disorder, not linked to sex, due to a mutation in the ATP7B gene, which generates changes in copper metabolism. It is a systemic disease characterized by hepatic, neurological and musculoskeletal disorders. Studies carried out with people affected by this disease in Brazil involved only the population of the south and southeast of the country. The aim of this study was to describe the central and peripheral neurological disorders in patients with Wilson's disease in the state of Ceará. 14 patients with a conclusive diagnosis of DW were recruited, accompanied by a neurologist at the Hospital Universitário Walter Cantídio (HUWC). Patients had their medical records reviewed; performed anamnesis, neurological evaluation, skin wrinkle test and answered the Quality of Life Determination (DEFU) questionnaires, Barthel Index and the Compound Score of Autonomic Symptoms (COMPASS 31). The mean age at the time of the patient survey was 39.4+ 2.61 years (25 to 53 years). All patients had neurological changes. Among these 8 had a positive family history of DW involving siblings, cousins and nephews, 10 patients had consanguineous parents and 6 lived in inland regions. The average age for the conclusive diagnosis of DW was 24.5 years ± 1.40 years (from 13 to 34 years). The most common neurological symptoms were: tremor, dysphagia, dysarthria, change in gait, stiffness, drooling, speech disorders and bradykinesia. The most common neurological signs were: tremor, cogwheel signal, Kayser Fleisher rings and Babinski signal. The most widely used pharmacological treatment was penicillamine. The most reported psychiatric symptom was depression. Among the evaluated patients, 71.4% (10) presented some symptom of autonomic dysfunction, of which 57% (8) obtained an abnormal result in the skin wrinkle test by immersing the hand in water. Among the neurological characteristics presented by the patients in this study, the involvement of sensitive and autonomic peripheral nerve fibers from the skin wrinkle test stands out. Our study proves the presence of peripheral neuropathy in 50% of patients affected with DW, as well as the correlation of this dysfunction with the presence of autonomic disorders.
publishDate 2021
dc.date.accessioned.fl_str_mv 2021-09-13T11:44:24Z
dc.date.available.fl_str_mv 2021-09-13T11:44:24Z
dc.date.issued.fl_str_mv 2021-06-18
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dc.identifier.citation.fl_str_mv SOBRINHO, J. Q. S. Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará. 2021. 175 f. Dissertação (Mestrado em Ciências Morfofuncionais) - Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, 2021.
dc.identifier.uri.fl_str_mv http://www.repositorio.ufc.br/handle/riufc/60405
identifier_str_mv SOBRINHO, J. Q. S. Estudo das alterações neurológicas centrais e periféricas em pacientes com doença de Wilson em um hospital universitário do estado do Ceará. 2021. 175 f. Dissertação (Mestrado em Ciências Morfofuncionais) - Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, 2021.
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