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J Clin Ultrasound ; 37(8): 471-4, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19655321

RESUMO

We report a case of a 23-year-old pregnant woman, who underwent amniocentesis after ultrasound (US) examination in the first trimester which revealed a nuchal translucency thickness of 2.9 mm. Cytogenetic analysis revealed complete tetrasomy of the short arm of chromosome 9. Further US evaluation in the second trimester revealed Dandy-Walker malformation, ventriculomegaly, bilateral clubfoot, lip and palate clefts, arthrogryposis and hyperechoic kidneys with bilateral pelvic dilatation. At 30 weeks of gestation, a placental abruption was noted and a Cesarean section was performed. The infant died shortly after birth. A review of previous cases of tetrasomy 9p shows that the remarkable sonographic findings are ventriculomegaly, intrauterine growth restriction, genitourinary anomaly, Dandy-Walker malformation, cleft lip/palate and limb malformation, but the association of tetrasomy 9p and increased nuchal translucency had not been reported.


Assuntos
Aberrações Cromossômicas , Cromossomos Humanos Par 9 , Síndrome de Dandy-Walker/diagnóstico por imagem , Medição da Translucência Nucal/métodos , Amniocentese , Síndrome de Dandy-Walker/genética , Diagnóstico Diferencial , Feminino , Humanos , Gravidez , Adulto Jovem
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