Craniofacial abnormalities among patients with Edwards Syndrome

Detalhes bibliográficos
Autor(a) principal: Rosa,Rafael Fabiano M.
Data de Publicação: 2013
Outros Autores: Rosa,Rosana Cardoso M., Lorenzen,Marina Boff, Zen,Paulo Ricardo G., Graziadio,Carla, Paskulin,Giorgio Adriano
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista Paulista de Pediatria (Ed. Português. Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822013000300293
Resumo: OBJECTIVE To determine the frequency and types of craniofacial abnormalities observed in patients with trisomy 18 or Edwards syndrome (ES). METHODS This descriptive and retrospective study of a case series included all patients diagnosed with ES in a Clinical Genetics Service of a reference hospital in Southern Brazil from 1975 to 2008. The results of the karyotypic analysis, along with clinical data, were collected from medical records. RESULTS: The sample consisted of 50 patients, of which 66% were female. The median age at first evaluation was 14 days. Regarding the karyotypes, full trisomy of chromosome 18 was the main alteration (90%). Mosaicism was observed in 10%. The main craniofacial abnormalities were: microretrognathia (76%), abnormalities of the ear helix/dysplastic ears (70%), prominent occiput (52%), posteriorly rotated (46%) and low set ears (44%), and short palpebral fissures/blepharophimosis (46%). Other uncommon - but relevant - abnormalities included: microtia (18%), orofacial clefts (12%), preauricular tags (10%), facial palsy (4%), encephalocele (4%), absence of external auditory canal (2%) and asymmetric face (2%). One patient had an initial suspicion of oculo-auriculo-vertebral spectrum (OAVS) or Goldenhar syndrome. CONCLUSIONS: Despite the literature description of a characteristic clinical presentation for ES, craniofacial alterations may be variable among these patients. The OAVS findings in this sample are noteworthy. The association of ES with OAVS has been reported once in the literature.
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spelling Craniofacial abnormalities among patients with Edwards Syndromechromosomes, human, pair 18trisomychromosome aberrationscraniofacial abnormalitiesGoldenhar syndrome OBJECTIVE To determine the frequency and types of craniofacial abnormalities observed in patients with trisomy 18 or Edwards syndrome (ES). METHODS This descriptive and retrospective study of a case series included all patients diagnosed with ES in a Clinical Genetics Service of a reference hospital in Southern Brazil from 1975 to 2008. The results of the karyotypic analysis, along with clinical data, were collected from medical records. RESULTS: The sample consisted of 50 patients, of which 66% were female. The median age at first evaluation was 14 days. Regarding the karyotypes, full trisomy of chromosome 18 was the main alteration (90%). Mosaicism was observed in 10%. The main craniofacial abnormalities were: microretrognathia (76%), abnormalities of the ear helix/dysplastic ears (70%), prominent occiput (52%), posteriorly rotated (46%) and low set ears (44%), and short palpebral fissures/blepharophimosis (46%). Other uncommon - but relevant - abnormalities included: microtia (18%), orofacial clefts (12%), preauricular tags (10%), facial palsy (4%), encephalocele (4%), absence of external auditory canal (2%) and asymmetric face (2%). One patient had an initial suspicion of oculo-auriculo-vertebral spectrum (OAVS) or Goldenhar syndrome. CONCLUSIONS: Despite the literature description of a characteristic clinical presentation for ES, craniofacial alterations may be variable among these patients. The OAVS findings in this sample are noteworthy. The association of ES with OAVS has been reported once in the literature. Sociedade de Pediatria de São Paulo2013-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822013000300293Revista Paulista de Pediatria v.31 n.3 2013reponame:Revista Paulista de Pediatria (Ed. Português. Online)instname:Sociedade de Pediatria de São Paulo (SPSP)instacron:SPSP10.1590/S0103-05822013000300004info:eu-repo/semantics/openAccessRosa,Rafael Fabiano M.Rosa,Rosana Cardoso M.Lorenzen,Marina BoffZen,Paulo Ricardo G.Graziadio,CarlaPaskulin,Giorgio Adrianoeng2015-07-31T00:00:00Zoai:scielo:S0103-05822013000300293Revistahttps://www.rpped.com.br/ONGhttps://old.scielo.br/oai/scielo-oai.phppediatria@spsp.org.br||rpp@spsp.org.br1984-04620103-0582opendoar:2015-07-31T00:00Revista Paulista de Pediatria (Ed. Português. Online) - Sociedade de Pediatria de São Paulo (SPSP)false
dc.title.none.fl_str_mv Craniofacial abnormalities among patients with Edwards Syndrome
title Craniofacial abnormalities among patients with Edwards Syndrome
spellingShingle Craniofacial abnormalities among patients with Edwards Syndrome
Rosa,Rafael Fabiano M.
chromosomes, human, pair 18
trisomy
chromosome aberrations
craniofacial abnormalities
Goldenhar syndrome
title_short Craniofacial abnormalities among patients with Edwards Syndrome
title_full Craniofacial abnormalities among patients with Edwards Syndrome
title_fullStr Craniofacial abnormalities among patients with Edwards Syndrome
title_full_unstemmed Craniofacial abnormalities among patients with Edwards Syndrome
title_sort Craniofacial abnormalities among patients with Edwards Syndrome
author Rosa,Rafael Fabiano M.
author_facet Rosa,Rafael Fabiano M.
Rosa,Rosana Cardoso M.
Lorenzen,Marina Boff
Zen,Paulo Ricardo G.
Graziadio,Carla
Paskulin,Giorgio Adriano
author_role author
author2 Rosa,Rosana Cardoso M.
Lorenzen,Marina Boff
Zen,Paulo Ricardo G.
Graziadio,Carla
Paskulin,Giorgio Adriano
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Rosa,Rafael Fabiano M.
Rosa,Rosana Cardoso M.
Lorenzen,Marina Boff
Zen,Paulo Ricardo G.
Graziadio,Carla
Paskulin,Giorgio Adriano
dc.subject.por.fl_str_mv chromosomes, human, pair 18
trisomy
chromosome aberrations
craniofacial abnormalities
Goldenhar syndrome
topic chromosomes, human, pair 18
trisomy
chromosome aberrations
craniofacial abnormalities
Goldenhar syndrome
description OBJECTIVE To determine the frequency and types of craniofacial abnormalities observed in patients with trisomy 18 or Edwards syndrome (ES). METHODS This descriptive and retrospective study of a case series included all patients diagnosed with ES in a Clinical Genetics Service of a reference hospital in Southern Brazil from 1975 to 2008. The results of the karyotypic analysis, along with clinical data, were collected from medical records. RESULTS: The sample consisted of 50 patients, of which 66% were female. The median age at first evaluation was 14 days. Regarding the karyotypes, full trisomy of chromosome 18 was the main alteration (90%). Mosaicism was observed in 10%. The main craniofacial abnormalities were: microretrognathia (76%), abnormalities of the ear helix/dysplastic ears (70%), prominent occiput (52%), posteriorly rotated (46%) and low set ears (44%), and short palpebral fissures/blepharophimosis (46%). Other uncommon - but relevant - abnormalities included: microtia (18%), orofacial clefts (12%), preauricular tags (10%), facial palsy (4%), encephalocele (4%), absence of external auditory canal (2%) and asymmetric face (2%). One patient had an initial suspicion of oculo-auriculo-vertebral spectrum (OAVS) or Goldenhar syndrome. CONCLUSIONS: Despite the literature description of a characteristic clinical presentation for ES, craniofacial alterations may be variable among these patients. The OAVS findings in this sample are noteworthy. The association of ES with OAVS has been reported once in the literature.
publishDate 2013
dc.date.none.fl_str_mv 2013-09-01
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://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822013000300293
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822013000300293
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-05822013000300004
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade de Pediatria de São Paulo
publisher.none.fl_str_mv Sociedade de Pediatria de São Paulo
dc.source.none.fl_str_mv Revista Paulista de Pediatria v.31 n.3 2013
reponame:Revista Paulista de Pediatria (Ed. Português. Online)
instname:Sociedade de Pediatria de São Paulo (SPSP)
instacron:SPSP
instname_str Sociedade de Pediatria de São Paulo (SPSP)
instacron_str SPSP
institution SPSP
reponame_str Revista Paulista de Pediatria (Ed. Português. Online)
collection Revista Paulista de Pediatria (Ed. Português. Online)
repository.name.fl_str_mv Revista Paulista de Pediatria (Ed. Português. Online) - Sociedade de Pediatria de São Paulo (SPSP)
repository.mail.fl_str_mv pediatria@spsp.org.br||rpp@spsp.org.br
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