Relato de caso de um paciente com mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy)
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Biblioteca Digital de Teses e Dissertações da USC |
Texto Completo: | http://localhost:8080/tede/handle/tede/120 |
Resumo: | Mucopolysaccharidosis (MPSs) are inherited metabolic diseases caused by a deficiency of lysosomal enzymes responsible for degradation of glycosaminoglycans, resulting in accumulation of these macromolecules within the lysosomes of cells,resulting in dysfunction of various organs and tissues in a progressive manner. A variation of this disease is a mucopolysaccharidosis (MPS) type VI or Maroteax-Lamy syndrome, in which the patient appears normal at birth but, in addition to the accumulation of MPSs arise progressive deformities such as short stature, coarse face, contractures joint, several skeletal defects, as well as cardiovascular,hepatoesplenomigalia, ocular, oral and speech therapy. This type of MPS does not have mental retardation and psychomotor retardation. This report presents some consequences arising from the speech therapy and dental syndrome, a carrier male with eight years of age. Physical examinations were performed, radiographic, speech therapy, dental, medical history and also collected information in the records of APAE. In examining speech, neurovegetative functions presented with bilateral chewing movements with anteroposterior and tongue. Presented short oral breathing (abdominal and thoracic), breathless and noisy. At the oral clinical examination,showed anterior open bite, macroglossia, tongue, but was not detected the presence of dental caries. In panoramic radiography, it was detected without the formation of five permanent teeth and images consistent with dentigerous cyst in the lower molars. Changes in stomatognathic systems and functions are prevalent in individuals with MPS type VI and these findings suggest that dental treatment and speech therapy has an important role in the quality of life of these individuals. |
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Francischone, Leda AparecidaCPF:06175983807http://lattes.cnpq.br/1423180913620381CPF:30337495858http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4231964A6Kumagai, Eliane Tiemi2015-09-14T13:12:43Z2011-12-092010-05-28KUMAGAI, Eliane Tiemi. Case report of a patient with mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome). 2010. 1 f. Dissertação (Mestrado em Biologia Oral) - IASCJ - Universidade Sagrado Coração, Bauru, 2010.http://localhost:8080/tede/handle/tede/120Mucopolysaccharidosis (MPSs) are inherited metabolic diseases caused by a deficiency of lysosomal enzymes responsible for degradation of glycosaminoglycans, resulting in accumulation of these macromolecules within the lysosomes of cells,resulting in dysfunction of various organs and tissues in a progressive manner. A variation of this disease is a mucopolysaccharidosis (MPS) type VI or Maroteax-Lamy syndrome, in which the patient appears normal at birth but, in addition to the accumulation of MPSs arise progressive deformities such as short stature, coarse face, contractures joint, several skeletal defects, as well as cardiovascular,hepatoesplenomigalia, ocular, oral and speech therapy. This type of MPS does not have mental retardation and psychomotor retardation. This report presents some consequences arising from the speech therapy and dental syndrome, a carrier male with eight years of age. Physical examinations were performed, radiographic, speech therapy, dental, medical history and also collected information in the records of APAE. In examining speech, neurovegetative functions presented with bilateral chewing movements with anteroposterior and tongue. Presented short oral breathing (abdominal and thoracic), breathless and noisy. At the oral clinical examination,showed anterior open bite, macroglossia, tongue, but was not detected the presence of dental caries. In panoramic radiography, it was detected without the formation of five permanent teeth and images consistent with dentigerous cyst in the lower molars. Changes in stomatognathic systems and functions are prevalent in individuals with MPS type VI and these findings suggest that dental treatment and speech therapy has an important role in the quality of life of these individuals.Mucopolissacaridoses (MPSs) são doenças metabólicas hereditárias causadas por uma deficiência de enzimas lisossomais, responsável pela degradação dos glicosaminoglicanos, ocasionando acúmulo dessas macromoléculas no interior dos lisossomos das células, resultando na disfunção de vários órgãos e tecidos de forma progressiva. Uma das variações dessa doença é a mucopolissacaridose (MPS) tipo VI, ou síndrome de Maroteax-Lamy, em que o portador se apresenta normal ao nascimento, mas, paralelamente ao acúmulo de MPSs, surgem deformidades progressivas como baixa estatura, face grosseira, contraturas articulares, diversos defeitos esqueléticos, assim como alterações cardiovasculares, hepatoesplenomigalia, oculares, fonoaudiológicas e bucais. Esse tipo de MPS não apresenta retardo mental e atraso psicomotor. Este relato de caso caracteriza algumas consequências fonoaudiológicas e odontológicas ocasionadas pela síndrome, de um portador do gênero masculino, com oito anos de idade. Foram realizados exames físico, radiográfico, fonoaudiológico, odontológico, anamnese e também colhetadas informações contidas no prontuário da APAE. No exame fonoaudiológico, as funções neurovegetativas apresentaram-se com a mastigação bilateral com movimentos anteroposterior e interposição lingual. Apresentou respiração bucal curta (abdominal e torácica), ofegante e com ruído. Ao exame clínico bucal, apresentou mordida aberta anterior, macroglossia, interposição lingual, mas não foi detectada a presença de cárie dentária. Na radiografia panorâmica, detectou-se ausência da formação de cinco dentes permanentes e imagens compatíveis com cisto dentígero nos molares inferiores. Alterações dos sistemas e funções estomatognáticas são prevalentes em indivíduos com MPS tipo VI e tais achados sugerem que o tratamento fonoterápico e odontológico tem um papel importante na qualidade de vida desses indivíduos.Made available in DSpace on 2015-09-14T13:12:43Z (GMT). No. of bitstreams: 1 dissertacao_eliane_kumagai.zip: 34991463 bytes, checksum: 0b00a3a4910643b078383395748daa1c (MD5) Previous issue date: 2010-05-28application/zipapplication/pdfporIASCJ - Universidade Sagrado CoraçãoBiologia OralUSCBRCiências da Saúde e BiológicasMUCOPOLISSACARIDOSESSÍNDROME DE MAROTEAUX-LAMYMUCOPOLYSACCHARIDOSISMAROTEAUX-LAMY SYNDROMECIENCIAS DA SAUDE::ODONTOLOGIARelato de caso de um paciente com mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy)Case report of a patient with mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome)info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis8043334104093724546600600600-753428887677182963-2070498469879244349info:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da USCinstname:Universidade do Sagrado Coração (USC)instacron:USCORIGINALdissertacao_eliane_kumagai.zipapplication/octet-stream34991463http://localhost:8080/tede/bitstream/tede/120/1/dissertacao_eliane_kumagai.zip0b00a3a4910643b078383395748daa1cMD51tede/1202015-10-19 09:11:09.967oai:localhost:tede/120Biblioteca Digital de Teses e Dissertaçõeshttps://tede2.usc.br:8443/http://tede2.usc.br:8080/oai/requestbiblicorjesu@unisagrado.edu.br||normalizacao@usc.bropendoar:2015-10-19T11:11:09Biblioteca Digital de Teses e Dissertações da USC - Universidade do Sagrado Coração (USC)false |
dc.title.por.fl_str_mv |
Relato de caso de um paciente com mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy) |
dc.title.alternative.eng.fl_str_mv |
Case report of a patient with mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome) |
title |
Relato de caso de um paciente com mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy) |
spellingShingle |
Relato de caso de um paciente com mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy) Kumagai, Eliane Tiemi MUCOPOLISSACARIDOSES SÍNDROME DE MAROTEAUX-LAMY MUCOPOLYSACCHARIDOSIS MAROTEAUX-LAMY SYNDROME CIENCIAS DA SAUDE::ODONTOLOGIA |
title_short |
Relato de caso de um paciente com mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy) |
title_full |
Relato de caso de um paciente com mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy) |
title_fullStr |
Relato de caso de um paciente com mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy) |
title_full_unstemmed |
Relato de caso de um paciente com mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy) |
title_sort |
Relato de caso de um paciente com mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy) |
author |
Kumagai, Eliane Tiemi |
author_facet |
Kumagai, Eliane Tiemi |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Francischone, Leda Aparecida |
dc.contributor.advisor1ID.fl_str_mv |
CPF:06175983807 |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/1423180913620381 |
dc.contributor.authorID.fl_str_mv |
CPF:30337495858 |
dc.contributor.authorLattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4231964A6 |
dc.contributor.author.fl_str_mv |
Kumagai, Eliane Tiemi |
contributor_str_mv |
Francischone, Leda Aparecida |
dc.subject.por.fl_str_mv |
MUCOPOLISSACARIDOSES SÍNDROME DE MAROTEAUX-LAMY |
topic |
MUCOPOLISSACARIDOSES SÍNDROME DE MAROTEAUX-LAMY MUCOPOLYSACCHARIDOSIS MAROTEAUX-LAMY SYNDROME CIENCIAS DA SAUDE::ODONTOLOGIA |
dc.subject.eng.fl_str_mv |
MUCOPOLYSACCHARIDOSIS MAROTEAUX-LAMY SYNDROME |
dc.subject.cnpq.fl_str_mv |
CIENCIAS DA SAUDE::ODONTOLOGIA |
description |
Mucopolysaccharidosis (MPSs) are inherited metabolic diseases caused by a deficiency of lysosomal enzymes responsible for degradation of glycosaminoglycans, resulting in accumulation of these macromolecules within the lysosomes of cells,resulting in dysfunction of various organs and tissues in a progressive manner. A variation of this disease is a mucopolysaccharidosis (MPS) type VI or Maroteax-Lamy syndrome, in which the patient appears normal at birth but, in addition to the accumulation of MPSs arise progressive deformities such as short stature, coarse face, contractures joint, several skeletal defects, as well as cardiovascular,hepatoesplenomigalia, ocular, oral and speech therapy. This type of MPS does not have mental retardation and psychomotor retardation. This report presents some consequences arising from the speech therapy and dental syndrome, a carrier male with eight years of age. Physical examinations were performed, radiographic, speech therapy, dental, medical history and also collected information in the records of APAE. In examining speech, neurovegetative functions presented with bilateral chewing movements with anteroposterior and tongue. Presented short oral breathing (abdominal and thoracic), breathless and noisy. At the oral clinical examination,showed anterior open bite, macroglossia, tongue, but was not detected the presence of dental caries. In panoramic radiography, it was detected without the formation of five permanent teeth and images consistent with dentigerous cyst in the lower molars. Changes in stomatognathic systems and functions are prevalent in individuals with MPS type VI and these findings suggest that dental treatment and speech therapy has an important role in the quality of life of these individuals. |
publishDate |
2010 |
dc.date.issued.fl_str_mv |
2010-05-28 |
dc.date.available.fl_str_mv |
2011-12-09 |
dc.date.accessioned.fl_str_mv |
2015-09-14T13:12:43Z |
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masterThesis |
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publishedVersion |
dc.identifier.citation.fl_str_mv |
KUMAGAI, Eliane Tiemi. Case report of a patient with mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome). 2010. 1 f. Dissertação (Mestrado em Biologia Oral) - IASCJ - Universidade Sagrado Coração, Bauru, 2010. |
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http://localhost:8080/tede/handle/tede/120 |
identifier_str_mv |
KUMAGAI, Eliane Tiemi. Case report of a patient with mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome). 2010. 1 f. Dissertação (Mestrado em Biologia Oral) - IASCJ - Universidade Sagrado Coração, Bauru, 2010. |
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