Lujan-Fryns Syndrome – familial recurrence in the same generation [Abstract in English]
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , , |
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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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 |
_version_ |
1809101749493956608 |