Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros

ABSTRACT: Objective: To report the case of two siblings with chronic granulomatous disease. Chronic granulomatous disease is a primary immunodeficiency disorder characterized by abnormal microbicidal activity. Mutations in the p47-phox gene (NCF-1) are present in about 30% of the patients with chron...

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Autores:
López Quintero, Juan Álvaro
Prando Andrade, Carolina
Agudelo Florez, Piedad
de Souza Paiva, Maria Aparecida
Costa Carvalho, Beatriz T.
Condino Neto, Antonio
Tipo de recurso:
Article of investigation
Fecha de publicación:
2004
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
por
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/45063
Acceso en línea:
https://hdl.handle.net/10495/45063
Palabra clave:
Enfermedad Granulomatosa Crónica
Granulomatous Disease, Chronic
https://id.nlm.nih.gov/mesh/D006105
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc-nd/2.5/co/
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dc.title.spa.fl_str_mv Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros
dc.title.translated.spa.fl_str_mv Autosomal chronic granulomatous disease: case report and mutation analysis of two Brazilian siblings
title Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros
spellingShingle Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros
Enfermedad Granulomatosa Crónica
Granulomatous Disease, Chronic
https://id.nlm.nih.gov/mesh/D006105
title_short Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros
title_full Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros
title_fullStr Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros
title_full_unstemmed Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros
title_sort Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros
dc.creator.fl_str_mv López Quintero, Juan Álvaro
Prando Andrade, Carolina
Agudelo Florez, Piedad
de Souza Paiva, Maria Aparecida
Costa Carvalho, Beatriz T.
Condino Neto, Antonio
dc.contributor.author.none.fl_str_mv López Quintero, Juan Álvaro
Prando Andrade, Carolina
Agudelo Florez, Piedad
de Souza Paiva, Maria Aparecida
Costa Carvalho, Beatriz T.
Condino Neto, Antonio
dc.contributor.researchgroup.spa.fl_str_mv Inmunodeficiencias Primarias
dc.subject.decs.none.fl_str_mv Enfermedad Granulomatosa Crónica
Granulomatous Disease, Chronic
topic Enfermedad Granulomatosa Crónica
Granulomatous Disease, Chronic
https://id.nlm.nih.gov/mesh/D006105
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D006105
description ABSTRACT: Objective: To report the case of two siblings with chronic granulomatous disease. Chronic granulomatous disease is a primary immunodeficiency disorder characterized by abnormal microbicidal activity. Mutations in the p47-phox gene (NCF-1) are present in about 30% of the patients with chronic granulomatous disease; this group presents a better prognosis and later onset of recurrent infections as compared with the X-linked variant, present in about 56% of patients. Description: Case 1 is a female presenting repeat infections since age 10, starting with impetigo followed by severe pneumonia six months later. The severity of the lung infection associated with liver abscess and the patient s resistance to treatment prompted laboratory investigation for immunodeficiency. The results of the nitroblue tetrazolium and superoxide release tests were consistent with a diagnosis of chronic granulomatous disease. The parents and siblings were assessed, revealing the presence of granulomatous disease in a brother (Case 2). He also presented repeat infections with impetigo at age 10, followed by pneumonia six months later, however in a non severe form. Single-strand conformational polymorphism analysis detected abnormal electrophoretic mobility of exon 2 of the NCF-1 gene. Sequence DNA analysis revealed a dinucleotide GT deletion in exon 2. Comments: It is important to evaluate the relatives of chronic granulomatous disease patients, even in the absence of typical clinical signs. Defining the mutation and its correlation with phenotype is important to provide appropriate genetic counseling and clinical prognosis.
publishDate 2004
dc.date.issued.none.fl_str_mv 2004
dc.date.accessioned.none.fl_str_mv 2025-02-19T23:35:48Z
dc.date.available.none.fl_str_mv 2025-02-19T23:35:48Z
dc.type.spa.fl_str_mv Reporte de caso
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dc.identifier.citation.spa.fl_str_mv Prando-Andrade C, Agudelo-Florez P, Lopez JA, Paiva MAS, Costa-Carvalho BT, Condino-Neto A. Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros. J Pediatr (Rio J). 2004;80:425-8.
dc.identifier.issn.none.fl_str_mv 0021-7557
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/45063
dc.identifier.eissn.none.fl_str_mv 1678-4782
identifier_str_mv Prando-Andrade C, Agudelo-Florez P, Lopez JA, Paiva MAS, Costa-Carvalho BT, Condino-Neto A. Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros. J Pediatr (Rio J). 2004;80:425-8.
0021-7557
1678-4782
url https://hdl.handle.net/10495/45063
dc.language.iso.spa.fl_str_mv eng
por
language eng
por
dc.relation.ispartofjournalabbrev.spa.fl_str_mv J. Pediatr.
dc.relation.citationendpage.spa.fl_str_mv 428
dc.relation.citationissue.spa.fl_str_mv 5
dc.relation.citationstartpage.spa.fl_str_mv 425
dc.relation.citationvolume.spa.fl_str_mv 80
dc.relation.ispartofjournal.spa.fl_str_mv Jornal de Pediatria
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dc.publisher.spa.fl_str_mv Sociedade Brasileira de Pediatria
dc.publisher.place.spa.fl_str_mv Río de Janeiro, Brasil
institution Universidad de Antioquia
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spelling López Quintero, Juan ÁlvaroPrando Andrade, CarolinaAgudelo Florez, Piedadde Souza Paiva, Maria AparecidaCosta Carvalho, Beatriz T.Condino Neto, AntonioInmunodeficiencias Primarias2025-02-19T23:35:48Z2025-02-19T23:35:48Z2004Prando-Andrade C, Agudelo-Florez P, Lopez JA, Paiva MAS, Costa-Carvalho BT, Condino-Neto A. Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileiros. J Pediatr (Rio J). 2004;80:425-8.0021-7557https://hdl.handle.net/10495/450631678-4782ABSTRACT: Objective: To report the case of two siblings with chronic granulomatous disease. Chronic granulomatous disease is a primary immunodeficiency disorder characterized by abnormal microbicidal activity. Mutations in the p47-phox gene (NCF-1) are present in about 30% of the patients with chronic granulomatous disease; this group presents a better prognosis and later onset of recurrent infections as compared with the X-linked variant, present in about 56% of patients. Description: Case 1 is a female presenting repeat infections since age 10, starting with impetigo followed by severe pneumonia six months later. The severity of the lung infection associated with liver abscess and the patient s resistance to treatment prompted laboratory investigation for immunodeficiency. The results of the nitroblue tetrazolium and superoxide release tests were consistent with a diagnosis of chronic granulomatous disease. The parents and siblings were assessed, revealing the presence of granulomatous disease in a brother (Case 2). He also presented repeat infections with impetigo at age 10, followed by pneumonia six months later, however in a non severe form. Single-strand conformational polymorphism analysis detected abnormal electrophoretic mobility of exon 2 of the NCF-1 gene. Sequence DNA analysis revealed a dinucleotide GT deletion in exon 2. Comments: It is important to evaluate the relatives of chronic granulomatous disease patients, even in the absence of typical clinical signs. Defining the mutation and its correlation with phenotype is important to provide appropriate genetic counseling and clinical prognosis.RESUMO: Objetivo: Relatar dois casos de irmãos com doença granulomatosa crônica. A doença granulomatosa crônica é uma imunodeficiência primária caracterizada por atividade microbicida deficiente. Mutações no gene que codifica a proteína p47-phox (NCF-1) estão presentes em 30% dos casos de doença granulomatosa crônica. Essa forma da doença é de herança autossômica recessiva e resulta em fenótipo de evolução mais benigno e início tardio em relação à forma ligada ao X, que corresponde a 56% dos casos. Descrição: Caso 1 - paciente feminina, iniciou infecções de repetição aos 10 anos, com impetigo, seguido de pneumonia grave 6 meses após. A gravidade da infecção pulmonar associada a abscesso hepático e sua refratariedade ao tratamento demandaram investigação laboratorial para imunodeficiência, com teste do nitroblue tetrazolium e dosagem de ânion superóxido compatíveis com doença granulomatosa crônica. A avaliação dos familiares confirmou o mesmo diagnóstico em seu irmão (Caso 2), que também iniciou infecções de repetição com impetigo aos 10 anos e pneumonia 6 meses após, porém tratada com sucesso ambulatorialmente. A análise de polimorfismo conformacional de cadeia simples revelou alteração da mobilidade eletroforética do éxon 2 do gene NCF-1. Identificou-se uma deleção dos nucleotídeos GT no éxon 2 por seqüenciamento do DNA. Comentários: Este estudo mostra a importância da avaliação de familiares, mesmo quando não apresentam história clínica típica de doença granulomatosa crônica. A identificação da mutação e sua correlação com o fenótipo dos pacientes é importante para estabelecer o prognóstico e o aconselhamento genético.COL00124264 páginasapplication/pdfengporSociedade Brasileira de PediatriaRío de Janeiro, Brasilhttp://creativecommons.org/licenses/by-nc-nd/2.5/co/https://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Doença granulomatosa crônica autossômica: relato de caso e análise genético-molecular de dois irmãos brasileirosAutosomal chronic granulomatous disease: case report and mutation analysis of two Brazilian siblingsReporte de casohttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARTCASOhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionEnfermedad Granulomatosa CrónicaGranulomatous Disease, Chronichttps://id.nlm.nih.gov/mesh/D006105J. 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