Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do CearÃ

Detalhes bibliográficos
Autor(a) principal: Leonardo Halley Carvalho Pimentel
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.
id UFC_346797d1a92b2e54cd7660a6690a4966
oai_identifier_str oai:www.teses.ufc.br:2087
network_acronym_str UFC
network_name_str Biblioteca Digital de Teses e Dissertações da UFC
spelling 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 CearÃ
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 CearÃ
spellingShingle Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do CearÃ
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 CearÃ
title_full Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do CearÃ
title_fullStr Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do CearÃ
title_full_unstemmed Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do CearÃ
title_sort Distrofias musculares progressivas de cinturas tipo 2: perfil epidemiolÃgico no estado do CearÃ
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 CearÃ
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 CearÃ
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
instacron_str UFC
institution UFC
repository.name.fl_str_mv -
repository.mail.fl_str_mv mail@mail.com
_version_ 1643295125177106432