Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do CearÃ
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Biblioteca Digital de Teses e Dissertações da UFC |
Texto Completo: | http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=2317 |
Resumo: | Objective: To report the clinical and muscle biopsy findings from the recessive forms of limb girdle muscular dystrophies (LGMD type 2) seen in the state of CearÃ, Northeast of Brazil. Design: Case series. Setting: Tertiary care clinic, University hospital. Patients and Methods: We studied 41 patients from 32 families with chronic progressive weakness in a limb-girdle distribution seen at a tertiary care hospital. All patients were born in the State of CearÃ. Patients with autossomal dominant pattern or facial involvement were excluded. Muscle biopsies specimens were immunostained for dystrophin, sarcoglycan, dysferlin, myotilin, merosin and emerin on all cases. Results: We found a specific protein deficiency in 24 patients (58.5%) from 20 families. Among these patients 11 (45.8%) had sarcoglycanopathy and 13 (54.2%) had dysferlinopathy and the pattern of inheritance was autosomal recessive or sporadic. Eletrocardiographic changes were seen in 6 (54.5%) patients with sarcoglycanopathy. Conclusion: Sarcoglicanopathies and disferlinopathies represent more than 60% of the cases of families with LGMD type 2 in this series from Northeast Brazil. Immunohistochemistry is still a very important tool for classification of LGMDs if genetic testing is not available or limited. Further studies are necessary to characterize the genetic background of the different LGMD families and to further characterize the other subtypes of LGMD type 2 in Brazil. |
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info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisDistrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do CearÃMuscular Dystrophies progressive of waists type 2: profile epidemiologist in the state of CearÃ, Northeast of Brazil 2008-09-26Carlos MaurÃcio de Castro Costa01356810306http://lattes.cnpq.br/9291210203141568 Francisco de Assis Aquino Gondim54844347349http://lattes.cnpq.br/1741899845739117Otoni Cardoso do Vale01404229353http://lattes.cnpq.br/0128019591224851 78034604372http://buscatextual.cnpq.br/buscatextual/visualizacv.jsp?id=K4267244D5Leonardo Halley Carvalho PimentelUniversidade Federal do CearÃPrograma de PÃs-GraduaÃÃo em FarmacologiaUFCBRDistrofia Muscular Progressiva de Cinturas Disferlinopatias Sarcoglicanopatias Nordeste Brasileiro Limb-girdle Muscular Dystrophies Dysferlinopathies Sarcoglycanopathies Northeast of BrazilFARMACOLOGIAObjective: To report the clinical and muscle biopsy findings from the recessive forms of limb girdle muscular dystrophies (LGMD type 2) seen in the state of CearÃ, Northeast of Brazil. Design: Case series. Setting: Tertiary care clinic, University hospital. Patients and Methods: We studied 41 patients from 32 families with chronic progressive weakness in a limb-girdle distribution seen at a tertiary care hospital. All patients were born in the State of CearÃ. Patients with autossomal dominant pattern or facial involvement were excluded. Muscle biopsies specimens were immunostained for dystrophin, sarcoglycan, dysferlin, myotilin, merosin and emerin on all cases. Results: We found a specific protein deficiency in 24 patients (58.5%) from 20 families. Among these patients 11 (45.8%) had sarcoglycanopathy and 13 (54.2%) had dysferlinopathy and the pattern of inheritance was autosomal recessive or sporadic. Eletrocardiographic changes were seen in 6 (54.5%) patients with sarcoglycanopathy. Conclusion: Sarcoglicanopathies and disferlinopathies represent more than 60% of the cases of families with LGMD type 2 in this series from Northeast Brazil. Immunohistochemistry is still a very important tool for classification of LGMDs if genetic testing is not available or limited. Further studies are necessary to characterize the genetic background of the different LGMD families and to further characterize the other subtypes of LGMD type 2 in Brazil. Objetivo: CaracterizaÃÃo clÃnica e de achados da biÃpsia muscular de formas recessivas de distrofias musculares de cinturas (DMPC tipo 2) no Estado do CearÃ, Nordeste do Brasil. Desenho: SÃrie de casos. Local: Hospital universitÃrio; atendimento terciÃrio. Pacientes e mÃtodos: Foram estudados 41 pacientes de 32 famÃlias com fraqueza crÃnica progressiva em distribuiÃÃo de cinturas atendidos em hospital terciÃrio. Todos os pacientes nasceram no Estado do CearÃ. Pacientes com padrÃo de heranÃa autossÃmico dominante ou com fraqueza facial foram excluÃdos. Os espÃcimes das biÃpsias musculares foram imunomarcados para distrofina, sarcoglicano, disferlina, miotilina, merosina e emerina em todos os casos. Resultados: Foi encontrado um padrÃo especÃfico de deficiÃncia protÃica em 24 pacientes (58,5%) de 20 famÃlias. Entre estes pacientes 11 (45,8%) tinham sarcoglicanopatia e 13 (54,2%) tinham disferlinopatia e o padrÃo de heranÃa foi recessivo ou esporÃdico. AlteraÃÃes eletrocardiogrÃficas foram observadas em 6 (54,5%) pacientes com sarcoglicanopatia. ConclusÃo: Sarcoglicanopatias e disferlinopatias representam mais de 60% dos casos de famÃlias com DMPC tipo 2 nesta sÃrie do Nosrdeste brasileiro. ImunohistoquÃmica ainda à uma ferramenta muito importante para classificaÃÃo das DMPCs se o teste genÃtico nÃo està disponÃvel ou à limitado. Estudos futuros sÃo necessÃrios para caracterizar o perfil genÃtico de diferentes famÃlias com DMPC, bem como caracterizar outros subtipos de DMPC tipo 2 no Brasil.CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superiorhttp://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=2317application/pdfinfo:eu-repo/semantics/openAccessporreponame:Biblioteca Digital de Teses e Dissertações da UFCinstname:Universidade Federal do Cearáinstacron:UFC2019-01-21T11:15:25Zmail@mail.com - |
dc.title.pt.fl_str_mv |
Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do Cearà |
dc.title.alternative..fl_str_mv |
Muscular Dystrophies progressive of waists type 2: profile epidemiologist in the state of CearÃ, Northeast of Brazil |
title |
Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do Cearà |
spellingShingle |
Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do Cearà Leonardo Halley Carvalho Pimentel Distrofia Muscular Progressiva de Cinturas Disferlinopatias Sarcoglicanopatias Nordeste Brasileiro Limb-girdle Muscular Dystrophies Dysferlinopathies Sarcoglycanopathies Northeast of Brazil FARMACOLOGIA |
title_short |
Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do Cearà |
title_full |
Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do Cearà |
title_fullStr |
Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do Cearà |
title_full_unstemmed |
Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do Cearà |
title_sort |
Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do Cearà |
author |
Leonardo Halley Carvalho Pimentel |
author_facet |
Leonardo Halley Carvalho Pimentel |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Carlos MaurÃcio de Castro Costa |
dc.contributor.advisor1ID.fl_str_mv |
01356810306 |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/9291210203141568 |
dc.contributor.referee1.fl_str_mv |
Francisco de Assis Aquino Gondim |
dc.contributor.referee1ID.fl_str_mv |
54844347349 |
dc.contributor.referee1Lattes.fl_str_mv |
http://lattes.cnpq.br/1741899845739117 |
dc.contributor.referee2.fl_str_mv |
Otoni Cardoso do Vale |
dc.contributor.referee2ID.fl_str_mv |
01404229353 |
dc.contributor.referee2Lattes.fl_str_mv |
http://lattes.cnpq.br/0128019591224851 |
dc.contributor.authorID.fl_str_mv |
78034604372 |
dc.contributor.authorLattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.jsp?id=K4267244D5 |
dc.contributor.author.fl_str_mv |
Leonardo Halley Carvalho Pimentel |
contributor_str_mv |
Carlos MaurÃcio de Castro Costa Francisco de Assis Aquino Gondim Otoni Cardoso do Vale |
dc.subject.por.fl_str_mv |
Distrofia Muscular Progressiva de Cinturas Disferlinopatias Sarcoglicanopatias Nordeste Brasileiro |
topic |
Distrofia Muscular Progressiva de Cinturas Disferlinopatias Sarcoglicanopatias Nordeste Brasileiro Limb-girdle Muscular Dystrophies Dysferlinopathies Sarcoglycanopathies Northeast of Brazil FARMACOLOGIA |
dc.subject.eng.fl_str_mv |
Limb-girdle Muscular Dystrophies Dysferlinopathies Sarcoglycanopathies Northeast of Brazil |
dc.subject.cnpq.fl_str_mv |
FARMACOLOGIA |
dc.description.sponsorship.fl_txt_mv |
CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior |
dc.description.abstract..fl_txt_mv |
Objective: To report the clinical and muscle biopsy findings from the recessive forms of limb girdle muscular dystrophies (LGMD type 2) seen in the state of CearÃ, Northeast of Brazil. Design: Case series. Setting: Tertiary care clinic, University hospital. Patients and Methods: We studied 41 patients from 32 families with chronic progressive weakness in a limb-girdle distribution seen at a tertiary care hospital. All patients were born in the State of CearÃ. Patients with autossomal dominant pattern or facial involvement were excluded. Muscle biopsies specimens were immunostained for dystrophin, sarcoglycan, dysferlin, myotilin, merosin and emerin on all cases. Results: We found a specific protein deficiency in 24 patients (58.5%) from 20 families. Among these patients 11 (45.8%) had sarcoglycanopathy and 13 (54.2%) had dysferlinopathy and the pattern of inheritance was autosomal recessive or sporadic. Eletrocardiographic changes were seen in 6 (54.5%) patients with sarcoglycanopathy. Conclusion: Sarcoglicanopathies and disferlinopathies represent more than 60% of the cases of families with LGMD type 2 in this series from Northeast Brazil. Immunohistochemistry is still a very important tool for classification of LGMDs if genetic testing is not available or limited. Further studies are necessary to characterize the genetic background of the different LGMD families and to further characterize the other subtypes of LGMD type 2 in Brazil. |
dc.description.abstract.por.fl_txt_mv |
Objetivo: CaracterizaÃÃo clÃnica e de achados da biÃpsia muscular de formas recessivas de distrofias musculares de cinturas (DMPC tipo 2) no Estado do CearÃ, Nordeste do Brasil. Desenho: SÃrie de casos. Local: Hospital universitÃrio; atendimento terciÃrio. Pacientes e mÃtodos: Foram estudados 41 pacientes de 32 famÃlias com fraqueza crÃnica progressiva em distribuiÃÃo de cinturas atendidos em hospital terciÃrio. Todos os pacientes nasceram no Estado do CearÃ. Pacientes com padrÃo de heranÃa autossÃmico dominante ou com fraqueza facial foram excluÃdos. Os espÃcimes das biÃpsias musculares foram imunomarcados para distrofina, sarcoglicano, disferlina, miotilina, merosina e emerina em todos os casos. Resultados: Foi encontrado um padrÃo especÃfico de deficiÃncia protÃica em 24 pacientes (58,5%) de 20 famÃlias. Entre estes pacientes 11 (45,8%) tinham sarcoglicanopatia e 13 (54,2%) tinham disferlinopatia e o padrÃo de heranÃa foi recessivo ou esporÃdico. AlteraÃÃes eletrocardiogrÃficas foram observadas em 6 (54,5%) pacientes com sarcoglicanopatia. ConclusÃo: Sarcoglicanopatias e disferlinopatias representam mais de 60% dos casos de famÃlias com DMPC tipo 2 nesta sÃrie do Nosrdeste brasileiro. ImunohistoquÃmica ainda à uma ferramenta muito importante para classificaÃÃo das DMPCs se o teste genÃtico nÃo està disponÃvel ou à limitado. Estudos futuros sÃo necessÃrios para caracterizar o perfil genÃtico de diferentes famÃlias com DMPC, bem como caracterizar outros subtipos de DMPC tipo 2 no Brasil. |
description |
Objective: To report the clinical and muscle biopsy findings from the recessive forms of limb girdle muscular dystrophies (LGMD type 2) seen in the state of CearÃ, Northeast of Brazil. Design: Case series. Setting: Tertiary care clinic, University hospital. Patients and Methods: We studied 41 patients from 32 families with chronic progressive weakness in a limb-girdle distribution seen at a tertiary care hospital. All patients were born in the State of CearÃ. Patients with autossomal dominant pattern or facial involvement were excluded. Muscle biopsies specimens were immunostained for dystrophin, sarcoglycan, dysferlin, myotilin, merosin and emerin on all cases. Results: We found a specific protein deficiency in 24 patients (58.5%) from 20 families. Among these patients 11 (45.8%) had sarcoglycanopathy and 13 (54.2%) had dysferlinopathy and the pattern of inheritance was autosomal recessive or sporadic. Eletrocardiographic changes were seen in 6 (54.5%) patients with sarcoglycanopathy. Conclusion: Sarcoglicanopathies and disferlinopathies represent more than 60% of the cases of families with LGMD type 2 in this series from Northeast Brazil. Immunohistochemistry is still a very important tool for classification of LGMDs if genetic testing is not available or limited. Further studies are necessary to characterize the genetic background of the different LGMD families and to further characterize the other subtypes of LGMD type 2 in Brazil. |
publishDate |
2008 |
dc.date.issued.fl_str_mv |
2008-09-26 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
status_str |
publishedVersion |
format |
masterThesis |
dc.identifier.uri.fl_str_mv |
http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=2317 |
url |
http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=2317 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal do Cearà |
dc.publisher.program.fl_str_mv |
Programa de PÃs-GraduaÃÃo em Farmacologia |
dc.publisher.initials.fl_str_mv |
UFC |
dc.publisher.country.fl_str_mv |
BR |
publisher.none.fl_str_mv |
Universidade Federal do Cearà |
dc.source.none.fl_str_mv |
reponame:Biblioteca Digital de Teses e Dissertações da UFC instname:Universidade Federal do Ceará instacron:UFC |
reponame_str |
Biblioteca Digital de Teses e Dissertações da UFC |
collection |
Biblioteca Digital de Teses e Dissertações da UFC |
instname_str |
Universidade Federal do Ceará |
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UFC |
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UFC |
repository.name.fl_str_mv |
-
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repository.mail.fl_str_mv |
mail@mail.com |
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1643295125177106432 |