Lujan-Fryns Syndrome – familial recurrence in the same generation [Abstract in English]

Detalhes bibliográficos
Autor(a) principal: Santos, Emerson Santana
Data de Publicação: 2011
Outros Autores: Costa, Fabiana Karla Aquino, Almeida, Danyelle Rego Barros, Ribeiro, Lásara Galvão, Barbosa, Moana Machado, Gomes, Rosamaria Rodrigues, Angelim, Vanessa Mont'Alverne Lopes
Tipo de documento: Artigo
Idioma: por
eng
Título da fonte: Scientia Medica (Porto Alegre. Online)
Texto Completo: https://revistaseletronicas.pucrs.br/scientiamedica/article/view/7640
Resumo: Aims: To report cases of Lujan-Fryns syndrome in two siblings. Description of cases: Patient 1 – male, 16 years, presented high stature, hiperextensibility of joints, prominent forehead, long face and narrow, maxillary hypoplasia, small jaw, large nose with high and narrow nasal bridge and short and deep filter, thin upper lip and arched palate, hypernasal voice and generalized hypotonia. Lability, learning disabilities, timidity and social phobia. Mitral valve prolapse with slight reflux and dilatation of the aortic root. Myopia without retinopathy. Karyotype in peripheral blood with G-band, molecular analysis for fragile X and biochemical investigation for homocystinuria had normal results. Patient 2 – female, 19 years, presented clinical symptoms similar to the patient 1 (her brother), although milder. Complementary tests showed no significant changes. Conclusions: These patients present marfanoid aspect and mental retardation consistent with X-linked inheritance. Although no research has been carried out on mutation in the gene MED 12, the clinical diagnosis of Lujan-Fryns syndrome is supported by the literature. There is no specific treatment, and the patients require special education and psychological counseling.
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spelling Lujan-Fryns Syndrome – familial recurrence in the same generation [Abstract in English]Síndrome de Lujan-Fryns – recorrência familiar na mesma geraçãoRARE DISEASES/GENETICSDIAGNOSISDIFFERENTIALMARFAN SYNDROME/DIAGNOSISMENTAL RETARDATIONX-LINKEDCHROMOSOME DISORDERSCASE REPORTS.DOENÇAS RARAS/GENÉTICADIAGNÓSTICO DIFERENCIALSÍNDROME DE MARFAN/DIAGNÓSTICORETARDO MENTAL LIGADO AO CROMOSSOMO XTRANSTORNOS CROMOSSÔMICOSRELATOS DE CASOS.Aims: To report cases of Lujan-Fryns syndrome in two siblings. Description of cases: Patient 1 – male, 16 years, presented high stature, hiperextensibility of joints, prominent forehead, long face and narrow, maxillary hypoplasia, small jaw, large nose with high and narrow nasal bridge and short and deep filter, thin upper lip and arched palate, hypernasal voice and generalized hypotonia. Lability, learning disabilities, timidity and social phobia. Mitral valve prolapse with slight reflux and dilatation of the aortic root. Myopia without retinopathy. Karyotype in peripheral blood with G-band, molecular analysis for fragile X and biochemical investigation for homocystinuria had normal results. Patient 2 – female, 19 years, presented clinical symptoms similar to the patient 1 (her brother), although milder. Complementary tests showed no significant changes. Conclusions: These patients present marfanoid aspect and mental retardation consistent with X-linked inheritance. Although no research has been carried out on mutation in the gene MED 12, the clinical diagnosis of Lujan-Fryns syndrome is supported by the literature. There is no specific treatment, and the patients require special education and psychological counseling.Objetivos: relatar casos da Síndrome de Lujan-Fryns em dois irmãos. Descrição dos casos: Paciente 1 – sexo masculino, 18 anos, apresentando alta estatura, hiperextensibilidade articular, região frontal proeminente, face longa e estreita, hipoplasia do maxilar, mandíbula pequena, nariz largo com ponte nasal alta e estreita, filtro curto e profundo, lábio superior fino e palato arqueado, voz hipernasal e hipotonia generalizada. Instabilidade emocional, distúrbio de aprendizagem, timidez e fobia social. Prolapso de válvula mitral com refluxo discreto e ectasia da raiz da aorta Miopia, sem retinopatia. Resultados normais para cariótipo em sangue periférico com banda G, análise molecular para X frágil e investigação para homocistinúria. Paciente 2 – sexo feminino, 22 anos, apresenta quadro clínico semelhante ao paciente 1 (seu irmão), porém de intensidade mais leve. Exames complementares sem alterações significativas. Conclusões: os pacientes apresentam aspecto marfanóide e retardo mental compatível com herança ligada ao X. Apesar de ainda não ter sido realizada a pesquisa da mutação no gene MED 12, o diagnóstico clínico de Síndrome de Lujan-Fryns está respaldado pela literatura. Não existe tratamento específico e os pacientes requerem educação especial e acompanhamento psicológico.Editora da PUCRS - ediPUCRS2011-06-29info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionRelato de caso raro ou de especial interesseapplication/pdfapplication/pdfhttps://revistaseletronicas.pucrs.br/scientiamedica/article/view/7640Scientia Medica; Vol. 21 No. 2 (2011); 64-66Scientia Medica; v. 21 n. 2 (2011); 64-661980-61081806-5562reponame:Scientia Medica (Porto Alegre. Online)instname:Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)instacron:PUC_RSporenghttps://revistaseletronicas.pucrs.br/scientiamedica/article/view/7640/6270https://revistaseletronicas.pucrs.br/scientiamedica/article/view/7640/6271Santos, Emerson SantanaCosta, Fabiana Karla AquinoAlmeida, Danyelle Rego BarrosRibeiro, Lásara GalvãoBarbosa, Moana MachadoGomes, Rosamaria RodriguesAngelim, Vanessa Mont'Alverne Lopesinfo:eu-repo/semantics/openAccess2013-07-16T12:00:20Zoai:ojs.revistaseletronicas.pucrs.br:article/7640Revistahttps://revistaseletronicas.pucrs.br/scientiamedica/PUBhttps://revistaseletronicas.pucrs.br/scientiamedica/oaiscientiamedica@pucrs.br || editora.periodicos@pucrs.br1980-61081806-5562opendoar:2013-07-16T12:00:20Scientia Medica (Porto Alegre. Online) - Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)false
dc.title.none.fl_str_mv Lujan-Fryns Syndrome – familial recurrence in the same generation [Abstract in English]
Síndrome de Lujan-Fryns – recorrência familiar na mesma geração
title Lujan-Fryns Syndrome – familial recurrence in the same generation [Abstract in English]
spellingShingle Lujan-Fryns Syndrome – familial recurrence in the same generation [Abstract in English]
Santos, Emerson Santana
RARE DISEASES/GENETICS
DIAGNOSIS
DIFFERENTIAL
MARFAN SYNDROME/DIAGNOSIS
MENTAL RETARDATION
X-LINKED
CHROMOSOME DISORDERS
CASE REPORTS.
DOENÇAS RARAS/GENÉTICA
DIAGNÓSTICO DIFERENCIAL
SÍNDROME DE MARFAN/DIAGNÓSTICO
RETARDO MENTAL LIGADO AO CROMOSSOMO X
TRANSTORNOS CROMOSSÔMICOS
RELATOS DE CASOS.
title_short Lujan-Fryns Syndrome – familial recurrence in the same generation [Abstract in English]
title_full Lujan-Fryns Syndrome – familial recurrence in the same generation [Abstract in English]
title_fullStr Lujan-Fryns Syndrome – familial recurrence in the same generation [Abstract in English]
title_full_unstemmed Lujan-Fryns Syndrome – familial recurrence in the same generation [Abstract in English]
title_sort Lujan-Fryns Syndrome – familial recurrence in the same generation [Abstract in English]
author Santos, Emerson Santana
author_facet Santos, Emerson Santana
Costa, Fabiana Karla Aquino
Almeida, Danyelle Rego Barros
Ribeiro, Lásara Galvão
Barbosa, Moana Machado
Gomes, Rosamaria Rodrigues
Angelim, Vanessa Mont'Alverne Lopes
author_role author
author2 Costa, Fabiana Karla Aquino
Almeida, Danyelle Rego Barros
Ribeiro, Lásara Galvão
Barbosa, Moana Machado
Gomes, Rosamaria Rodrigues
Angelim, Vanessa Mont'Alverne Lopes
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Santos, Emerson Santana
Costa, Fabiana Karla Aquino
Almeida, Danyelle Rego Barros
Ribeiro, Lásara Galvão
Barbosa, Moana Machado
Gomes, Rosamaria Rodrigues
Angelim, Vanessa Mont'Alverne Lopes
dc.subject.por.fl_str_mv RARE DISEASES/GENETICS
DIAGNOSIS
DIFFERENTIAL
MARFAN SYNDROME/DIAGNOSIS
MENTAL RETARDATION
X-LINKED
CHROMOSOME DISORDERS
CASE REPORTS.
DOENÇAS RARAS/GENÉTICA
DIAGNÓSTICO DIFERENCIAL
SÍNDROME DE MARFAN/DIAGNÓSTICO
RETARDO MENTAL LIGADO AO CROMOSSOMO X
TRANSTORNOS CROMOSSÔMICOS
RELATOS DE CASOS.
topic RARE DISEASES/GENETICS
DIAGNOSIS
DIFFERENTIAL
MARFAN SYNDROME/DIAGNOSIS
MENTAL RETARDATION
X-LINKED
CHROMOSOME DISORDERS
CASE REPORTS.
DOENÇAS RARAS/GENÉTICA
DIAGNÓSTICO DIFERENCIAL
SÍNDROME DE MARFAN/DIAGNÓSTICO
RETARDO MENTAL LIGADO AO CROMOSSOMO X
TRANSTORNOS CROMOSSÔMICOS
RELATOS DE CASOS.
description Aims: To report cases of Lujan-Fryns syndrome in two siblings. Description of cases: Patient 1 – male, 16 years, presented high stature, hiperextensibility of joints, prominent forehead, long face and narrow, maxillary hypoplasia, small jaw, large nose with high and narrow nasal bridge and short and deep filter, thin upper lip and arched palate, hypernasal voice and generalized hypotonia. Lability, learning disabilities, timidity and social phobia. Mitral valve prolapse with slight reflux and dilatation of the aortic root. Myopia without retinopathy. Karyotype in peripheral blood with G-band, molecular analysis for fragile X and biochemical investigation for homocystinuria had normal results. Patient 2 – female, 19 years, presented clinical symptoms similar to the patient 1 (her brother), although milder. Complementary tests showed no significant changes. Conclusions: These patients present marfanoid aspect and mental retardation consistent with X-linked inheritance. Although no research has been carried out on mutation in the gene MED 12, the clinical diagnosis of Lujan-Fryns syndrome is supported by the literature. There is no specific treatment, and the patients require special education and psychological counseling.
publishDate 2011
dc.date.none.fl_str_mv 2011-06-29
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Relato de caso raro ou de especial interesse
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://revistaseletronicas.pucrs.br/scientiamedica/article/view/7640
url https://revistaseletronicas.pucrs.br/scientiamedica/article/view/7640
dc.language.iso.fl_str_mv por
eng
language por
eng
dc.relation.none.fl_str_mv https://revistaseletronicas.pucrs.br/scientiamedica/article/view/7640/6270
https://revistaseletronicas.pucrs.br/scientiamedica/article/view/7640/6271
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Editora da PUCRS - ediPUCRS
publisher.none.fl_str_mv Editora da PUCRS - ediPUCRS
dc.source.none.fl_str_mv Scientia Medica; Vol. 21 No. 2 (2011); 64-66
Scientia Medica; v. 21 n. 2 (2011); 64-66
1980-6108
1806-5562
reponame:Scientia Medica (Porto Alegre. Online)
instname:Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
instacron:PUC_RS
instname_str Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
instacron_str PUC_RS
institution PUC_RS
reponame_str Scientia Medica (Porto Alegre. Online)
collection Scientia Medica (Porto Alegre. Online)
repository.name.fl_str_mv Scientia Medica (Porto Alegre. Online) - Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
repository.mail.fl_str_mv scientiamedica@pucrs.br || editora.periodicos@pucrs.br
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