Análise da expressão do colágeno VI na distrofia muscular congênita
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , , |
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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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 |
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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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1814268379121319936 |