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Prenat Diagn ; 34(2): 163-7, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24218399

RESUMO

OBJECTIVES: Cornelia de Lange syndrome (CdLS) is characterized by distinct facial features, growth retardation, upper limb reduction defects, hirsutism, and intellectual disability. NIPBL mutations have been identified in approximately 60% of patients with CdLS diagnosed postnatally. Prenatal ultrasound findings include upper limb reduction defects, intrauterine growth restriction, and micrognathia. CdLS has also been associated with decreased PAPP-A and increased nuchal translucency (NT). We reviewed NIPBL sequence analysis results for 12 prenatal samples in our laboratory to determine the frequency of mutations in our cohort. METHODS: This retrospective study analyzed data from all 12 prenatal cases with suspected CdLS, which were received by The University of Chicago Genetic Services Laboratories. Diagnostic NIPBL sequencing was performed for all samples. Clinical information was collected from referring physicians. RESULTS: NIPBL mutations were identified in 9 out of the 12 cases prenatally (75%). Amongst the NIPBL mutation-positive cases with clinical information available, the most common findings were upper limb malformations and micrognathia. Five patients had NT measurements in the first trimester, of which four were noted to be increased. CONCLUSION: We demonstrate that prenatally-detected phenotypes of CdLS, particularly severe micrognathia and bilateral upper limb defects, are associated with an increased frequency of NIPBL mutations.


Assuntos
Síndrome de Cornélia de Lange/genética , Micrognatismo/diagnóstico por imagem , Proteínas/genética , Deformidades Congênitas das Extremidades Superiores/diagnóstico por imagem , Proteínas de Ciclo Celular , Estudos de Coortes , Síndrome de Cornélia de Lange/complicações , Síndrome de Cornélia de Lange/diagnóstico por imagem , Feminino , Humanos , Recém-Nascido , Micrognatismo/etiologia , Mutação , Medição da Translucência Nucal , Gravidez , Diagnóstico Pré-Natal , Estudos Retrospectivos , Análise de Sequência de DNA , Ultrassonografia Pré-Natal , Deformidades Congênitas das Extremidades Superiores/etiologia
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