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...
- Autores:
- Tipo de recurso:
- 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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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 |
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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 |
dc.relation.uri.spa.fl_str_mv |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84859042559&partnerID=40&md5=5626cd84766912b4707a36e6c2c57b09 |
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http://purl.org/coar/access_right/c_abf2 |
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Abierto (Texto Completo) |
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Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
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