Análise da expressão do colágeno VI na distrofia muscular congênita

Detalhes bibliográficos
Autor(a) principal: Freitas, Regina Toni Loureiro de [UNIFESP]
Data de Publicação: 2005
Outros Autores: Zanoteli, Edmar [UNIFESP], Morita, Maria Da Penha Ananias [UNIFESP], Oliveira, Acary Souza Bulle [UNIFESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0004-282X2005000300027
http://repositorio.unifesp.br/handle/11600/2544
Resumo: Congenital muscular dystrophy (CMD) composes a group of disorders characterized by hypotonia and muscular weakness noticed in the first year of life. The Ullrich's form is characterized by proximal joint contractures and distal hiperextensibility. About 40% of these patients present mutations in one of the genes that codify the sub-units of the collagen VI protein (COL6), producing total or partial deficiency of the protein expression. We analyzed, through immunohistochemistry, the expression of COL6 in muscle fragments of 50 patients with CMD; 20 of them presented merosin expression deficiency. We identified 4 cases with total COL6 deficiency (8% of the total), representing 13% of the cases with normal merosin expression. The histological findings of patients with deficiency of COL6 were indistinguishable from other forms of CMD, but milder than that abnormalities observed in merosin deficient patients. In three COL6 deficient patients were observed hypotonia and weakness in the neonatal period, delayed of motor milestones, muscular retractions of knees and elbows, distal joint hiperextensibility and congenital hip dislocation (two patients). One patient lost the ability to walk; and one died due to respiratory problems. The analysis of COL6 expression, as well as merosin expression, in the muscle tissue from CMD patients, can be important for identification and phenotypic characterization of different CMD subtypes.
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spelling Análise da expressão do colágeno VI na distrofia muscular congênitaAnalysis of the expression of collagen VI in congenital muscular dystrophytype VI collagencongenital muscular dystrophyimmunohistochemistrycolágeno tipo VIdistrofia muscular congênitaimunofluorescênciaCongenital muscular dystrophy (CMD) composes a group of disorders characterized by hypotonia and muscular weakness noticed in the first year of life. The Ullrich's form is characterized by proximal joint contractures and distal hiperextensibility. About 40% of these patients present mutations in one of the genes that codify the sub-units of the collagen VI protein (COL6), producing total or partial deficiency of the protein expression. We analyzed, through immunohistochemistry, the expression of COL6 in muscle fragments of 50 patients with CMD; 20 of them presented merosin expression deficiency. We identified 4 cases with total COL6 deficiency (8% of the total), representing 13% of the cases with normal merosin expression. The histological findings of patients with deficiency of COL6 were indistinguishable from other forms of CMD, but milder than that abnormalities observed in merosin deficient patients. In three COL6 deficient patients were observed hypotonia and weakness in the neonatal period, delayed of motor milestones, muscular retractions of knees and elbows, distal joint hiperextensibility and congenital hip dislocation (two patients). One patient lost the ability to walk; and one died due to respiratory problems. The analysis of COL6 expression, as well as merosin expression, in the muscle tissue from CMD patients, can be important for identification and phenotypic characterization of different CMD subtypes.A distrofia muscular congênita (DMC) compõe um grupo de miopatias caracterizadas por hipotonia e fraqueza muscular notadas já no primeiro ano de vida. A forma de Ullrich é caracterizada por retrações musculares proximais e hiperextensibilidade distal. Cerca de 40% destes pacientes apresentam mutações em um dos genes que codificam as três sub-unidades do colágeno VI (COL6), acarretando deficiência total ou parcial na marcação da proteína. Analisamos, através de imunofluorescência, a marcação do COL6 em fragmentos musculares de 50 pacientes com DMC, 20 deles com ausência da marcação para merosina. Identificamos 4 casos com deficiência total da marcação do COL6 (8% do total), representando 13% dos casos com marcação normal para merosina. As alterações histológicas musculares dos pacientes com COL6 deficiente eram indistinguíveis das outras formas de DMC, porém mais brandas que as observadas na DMC com deficiência de merosina. Em três dos pacientes com COL6 deficiente observou-se hipotonia e fraqueza muscular, notadas já no período neonatal, atraso do desenvolvimento motor, retrações musculares em joelhos e cotovelos, hiperextensibilidade distal e luxação congênita do quadril (dois pacientes). Um paciente perdeu a capacidade para a marcha, e outro faleceu por problemas respiratórios. A análise da marcação do COL6, assim como da merosina, no tecido muscular de pacientes com DMC pode auxiliar na identificação e caracterização fenotípica dos diversos subtipos de DMC.UNIFESP-EPMUNIFESP-EPM Setor de Investigação em Doenças NeuromuscularesUNIFESP, EPM, Setor de Investigação em Doenças NeuromuscularesSciELOAcademia Brasileira de Neurologia - ABNEUROUniversidade Federal de São Paulo (UNIFESP)Freitas, Regina Toni Loureiro de [UNIFESP]Zanoteli, Edmar [UNIFESP]Morita, Maria Da Penha Ananias [UNIFESP]Oliveira, Acary Souza Bulle [UNIFESP]2015-06-14T13:31:36Z2015-06-14T13:31:36Z2005-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion514-518application/pdfhttp://dx.doi.org/10.1590/S0004-282X2005000300027Arquivos de Neuro-Psiquiatria. Academia Brasileira de Neurologia - ABNEURO, v. 63, n. 2b, p. 514-518, 2005.10.1590/S0004-282X2005000300027S0004-282X2005000300027.pdf0004-282XS0004-282X2005000300027http://repositorio.unifesp.br/handle/11600/2544WOS:000230309800027porArquivos de Neuro-Psiquiatriainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-04T13:48:38Zoai:repositorio.unifesp.br/:11600/2544Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-04T13:48:38Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Análise da expressão do colágeno VI na distrofia muscular congênita
Analysis of the expression of collagen VI in congenital muscular dystrophy
title Análise da expressão do colágeno VI na distrofia muscular congênita
spellingShingle Análise da expressão do colágeno VI na distrofia muscular congênita
Freitas, Regina Toni Loureiro de [UNIFESP]
type VI collagen
congenital muscular dystrophy
immunohistochemistry
colágeno tipo VI
distrofia muscular congênita
imunofluorescência
title_short Análise da expressão do colágeno VI na distrofia muscular congênita
title_full Análise da expressão do colágeno VI na distrofia muscular congênita
title_fullStr Análise da expressão do colágeno VI na distrofia muscular congênita
title_full_unstemmed Análise da expressão do colágeno VI na distrofia muscular congênita
title_sort Análise da expressão do colágeno VI na distrofia muscular congênita
author Freitas, Regina Toni Loureiro de [UNIFESP]
author_facet Freitas, Regina Toni Loureiro de [UNIFESP]
Zanoteli, Edmar [UNIFESP]
Morita, Maria Da Penha Ananias [UNIFESP]
Oliveira, Acary Souza Bulle [UNIFESP]
author_role author
author2 Zanoteli, Edmar [UNIFESP]
Morita, Maria Da Penha Ananias [UNIFESP]
Oliveira, Acary Souza Bulle [UNIFESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Freitas, Regina Toni Loureiro de [UNIFESP]
Zanoteli, Edmar [UNIFESP]
Morita, Maria Da Penha Ananias [UNIFESP]
Oliveira, Acary Souza Bulle [UNIFESP]
dc.subject.por.fl_str_mv type VI collagen
congenital muscular dystrophy
immunohistochemistry
colágeno tipo VI
distrofia muscular congênita
imunofluorescência
topic type VI collagen
congenital muscular dystrophy
immunohistochemistry
colágeno tipo VI
distrofia muscular congênita
imunofluorescência
description Congenital muscular dystrophy (CMD) composes a group of disorders characterized by hypotonia and muscular weakness noticed in the first year of life. The Ullrich's form is characterized by proximal joint contractures and distal hiperextensibility. About 40% of these patients present mutations in one of the genes that codify the sub-units of the collagen VI protein (COL6), producing total or partial deficiency of the protein expression. We analyzed, through immunohistochemistry, the expression of COL6 in muscle fragments of 50 patients with CMD; 20 of them presented merosin expression deficiency. We identified 4 cases with total COL6 deficiency (8% of the total), representing 13% of the cases with normal merosin expression. The histological findings of patients with deficiency of COL6 were indistinguishable from other forms of CMD, but milder than that abnormalities observed in merosin deficient patients. In three COL6 deficient patients were observed hypotonia and weakness in the neonatal period, delayed of motor milestones, muscular retractions of knees and elbows, distal joint hiperextensibility and congenital hip dislocation (two patients). One patient lost the ability to walk; and one died due to respiratory problems. The analysis of COL6 expression, as well as merosin expression, in the muscle tissue from CMD patients, can be important for identification and phenotypic characterization of different CMD subtypes.
publishDate 2005
dc.date.none.fl_str_mv 2005-06-01
2015-06-14T13:31:36Z
2015-06-14T13:31:36Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0004-282X2005000300027
Arquivos de Neuro-Psiquiatria. Academia Brasileira de Neurologia - ABNEURO, v. 63, n. 2b, p. 514-518, 2005.
10.1590/S0004-282X2005000300027
S0004-282X2005000300027.pdf
0004-282X
S0004-282X2005000300027
http://repositorio.unifesp.br/handle/11600/2544
WOS:000230309800027
url http://dx.doi.org/10.1590/S0004-282X2005000300027
http://repositorio.unifesp.br/handle/11600/2544
identifier_str_mv Arquivos de Neuro-Psiquiatria. Academia Brasileira de Neurologia - ABNEURO, v. 63, n. 2b, p. 514-518, 2005.
10.1590/S0004-282X2005000300027
S0004-282X2005000300027.pdf
0004-282X
S0004-282X2005000300027
WOS:000230309800027
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Arquivos de Neuro-Psiquiatria
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 514-518
application/pdf
dc.publisher.none.fl_str_mv Academia Brasileira de Neurologia - ABNEURO
publisher.none.fl_str_mv Academia Brasileira de Neurologia - ABNEURO
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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