Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease

Cardiac defects are the most frequent congenital malformations, with an incidence estimated between 4 and 12 per 1000 newborns. Their etiology is multifactorial and might be attributed to genetic predispositions and environmental factors. Since 1990 these types of pathologies have been associated wi...

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Fecha de publicación:
2011
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/22190
Acceso en línea:
https://repository.urosario.edu.co/handle/10336/22190
Palabra clave:
Article
Chromosome deletion 22q11
Congenital heart disease
Fallot tetralogy
Genetic association
Heart atrium septum defect
Human
Major clinical study
Adolescent
Adult
Child
Chromosome deletion
Colombia
Dna mutational analysis
Female
Gene frequency
Genetic predisposition to disease
Humans
Infant
Male
Tetralogy of fallot
Young adult
Atrial septal defects
Congenital heart diseases
Densitometry
Microdeletion 22q11
Multiplex pcr
Tetralogy of fallot
Tuple 1
newborn
congenital
atrial
preschool
human
pair 22
Child
Chromosomes
Heart defects
Heart septal defects
Infant
Rights
License
Abierto (Texto Completo)
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spelling 16fbf46c-9f2f-4e74-94e1-c5a8926ae6e3bb3281e3-8d33-43be-9c1b-f58ae9e01d001c0cc46b-fb53-42ee-a06e-e0133b0b50b33152755060052094825600fc87266a-2304-446d-aece-15bfeb085858d95184da-7ac8-4be8-a3c0-3ab964d09bd56852c819-f849-4c68-bf5f-b28d69f64d7b62923368-3266-47ae-92fb-f249117680aa2020-05-25T23:55:43Z2020-05-25T23:55:43Z2011Cardiac defects are the most frequent congenital malformations, with an incidence estimated between 4 and 12 per 1000 newborns. Their etiology is multifactorial and might be attributed to genetic predispositions and environmental factors. Since 1990 these types of pathologies have been associated with 22q11 microdeletion. In this study, the frequency of microdeletion 22q11 was determined in 61 patients with non-syndromic congenital heart disease. DNA was extracted from peripheral blood and TUPLE1 and STR D10S2198 genes were amplified by multiplex PCR and visualized in agarose gels. Gene content was quantified by densitometry. Three patients were found with microdeletion 22q11, representing a 4.9% frequency. This microdeletion was associated with two cases of Tetralogy of Fallot and a third case with atrial septal defect (ASD). In conclusion, the frequency for microdeletion 22q11 in the population analyzed was 4.9%. The cases that presented Teratology of Fallot had a frequency for this microdeletion of 7.4% and for ASD of 11.1%.application/pdf5355133https://repository.urosario.edu.co/handle/10336/22190eng343No. 4334Investigacion ClinicaVol. 52Investigacion Clinica, ISSN:5355133, Vol.52, No.4 (2011); pp. 334-343https://www.scopus.com/inward/record.uri?eid=2-s2.0-84859042559&partnerID=40&md5=5626cd84766912b4707a36e6c2c57b09Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURArticleChromosome deletion 22q11Congenital heart diseaseFallot tetralogyGenetic associationHeart atrium septum defectHumanMajor clinical studyAdolescentAdultChildChromosome deletionColombiaDna mutational analysisFemaleGene frequencyGenetic predisposition to diseaseHumansInfantMaleTetralogy of fallotYoung adultAtrial septal defectsCongenital heart diseasesDensitometryMicrodeletion 22q11Multiplex pcrTetralogy of fallotTuple 1newborncongenitalatrialpreschoolhumanpair 22ChildChromosomesHeart defectsHeart septal defectsInfantAnalysis of microdeletions in 22q11 in Colombian patients with congenital heart diseaseAnálisis de microdeleciones en 22q11 en pacientes colombianos con cardiopatía congénita no sindrómicaarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Salazar M.Villalba G.Mateus H.Villegas Gálvez, Victoria EugeniaFonseca Mendoza, Dora JanethNúñez F.Caicedo V.Pachón S.Bernal J.E.ORIGINAL372937686005.pdfapplication/pdf127337https://repository.urosario.edu.co/bitstreams/8eb1a4ea-4bda-4e6a-a814-45c24addea86/downloade223d18d1148c4ccc77603bc48050328MD51TEXT372937686005.pdf.txt372937686005.pdf.txtExtracted texttext/plain31380https://repository.urosario.edu.co/bitstreams/9349b1e6-7291-4c17-b726-15ac2441d303/downloadc2fcad9bd0fa7e54529747690ac9d7c1MD52THUMBNAIL372937686005.pdf.jpg372937686005.pdf.jpgGenerated Thumbnailimage/jpeg2405https://repository.urosario.edu.co/bitstreams/b6ede028-6bbd-4197-949a-8493c4aa9a20/download1f2c22f5991df167ce5eaf063856f69eMD5310336/22190oai:repository.urosario.edu.co:10336/221902022-05-02 07:37:17.706705https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease
dc.title.TranslatedTitle.spa.fl_str_mv Análisis de microdeleciones en 22q11 en pacientes colombianos con cardiopatía congénita no sindrómica
title Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease
spellingShingle Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease
Article
Chromosome deletion 22q11
Congenital heart disease
Fallot tetralogy
Genetic association
Heart atrium septum defect
Human
Major clinical study
Adolescent
Adult
Child
Chromosome deletion
Colombia
Dna mutational analysis
Female
Gene frequency
Genetic predisposition to disease
Humans
Infant
Male
Tetralogy of fallot
Young adult
Atrial septal defects
Congenital heart diseases
Densitometry
Microdeletion 22q11
Multiplex pcr
Tetralogy of fallot
Tuple 1
newborn
congenital
atrial
preschool
human
pair 22
Child
Chromosomes
Heart defects
Heart septal defects
Infant
title_short Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease
title_full Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease
title_fullStr Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease
title_full_unstemmed Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease
title_sort Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease
dc.subject.keyword.spa.fl_str_mv Article
Chromosome deletion 22q11
Congenital heart disease
Fallot tetralogy
Genetic association
Heart atrium septum defect
Human
Major clinical study
Adolescent
Adult
Child
Chromosome deletion
Colombia
Dna mutational analysis
Female
Gene frequency
Genetic predisposition to disease
Humans
Infant
Male
Tetralogy of fallot
Young adult
Atrial septal defects
Congenital heart diseases
Densitometry
Microdeletion 22q11
Multiplex pcr
Tetralogy of fallot
Tuple 1
topic Article
Chromosome deletion 22q11
Congenital heart disease
Fallot tetralogy
Genetic association
Heart atrium septum defect
Human
Major clinical study
Adolescent
Adult
Child
Chromosome deletion
Colombia
Dna mutational analysis
Female
Gene frequency
Genetic predisposition to disease
Humans
Infant
Male
Tetralogy of fallot
Young adult
Atrial septal defects
Congenital heart diseases
Densitometry
Microdeletion 22q11
Multiplex pcr
Tetralogy of fallot
Tuple 1
newborn
congenital
atrial
preschool
human
pair 22
Child
Chromosomes
Heart defects
Heart septal defects
Infant
dc.subject.keyword.eng.fl_str_mv newborn
congenital
atrial
preschool
human
pair 22
Child
Chromosomes
Heart defects
Heart septal defects
Infant
description Cardiac defects are the most frequent congenital malformations, with an incidence estimated between 4 and 12 per 1000 newborns. Their etiology is multifactorial and might be attributed to genetic predispositions and environmental factors. Since 1990 these types of pathologies have been associated with 22q11 microdeletion. In this study, the frequency of microdeletion 22q11 was determined in 61 patients with non-syndromic congenital heart disease. DNA was extracted from peripheral blood and TUPLE1 and STR D10S2198 genes were amplified by multiplex PCR and visualized in agarose gels. Gene content was quantified by densitometry. Three patients were found with microdeletion 22q11, representing a 4.9% frequency. This microdeletion was associated with two cases of Tetralogy of Fallot and a third case with atrial septal defect (ASD). In conclusion, the frequency for microdeletion 22q11 in the population analyzed was 4.9%. The cases that presented Teratology of Fallot had a frequency for this microdeletion of 7.4% and for ASD of 11.1%.
publishDate 2011
dc.date.created.spa.fl_str_mv 2011
dc.date.accessioned.none.fl_str_mv 2020-05-25T23:55:43Z
dc.date.available.none.fl_str_mv 2020-05-25T23:55:43Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.issn.none.fl_str_mv 5355133
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/22190
identifier_str_mv 5355133
url https://repository.urosario.edu.co/handle/10336/22190
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 343
dc.relation.citationIssue.none.fl_str_mv No. 4
dc.relation.citationStartPage.none.fl_str_mv 334
dc.relation.citationTitle.none.fl_str_mv Investigacion Clinica
dc.relation.citationVolume.none.fl_str_mv Vol. 52
dc.relation.ispartof.spa.fl_str_mv Investigacion Clinica, ISSN:5355133, Vol.52, No.4 (2011); pp. 334-343
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