Prenatal diagnosis of Dandy-Walker syndrome in early pregnancy presenting with increased nuchal translucency and generalized edema at 13 weeks of gestation.

نویسندگان

  • Sheng Hsien Chen
  • Mike Yan-Sheng Lin
  • Fong-Ming Chang
چکیده

Chang CH, Chang FM, Yu CH, Liang RI, Ko HC, Chen HY. 2000. Fetal ear assessment and prenatal detection of aneuploidy by the quantitative three-dimensional ultrasonography. Ultrasound Med Biol 26: 743–749. Chang LW, Chang FM, Chang CH, Yu CH, Cheng YC, Chen HY. 2002. Prenatal diagnosis of fetal multicystic dysplastic kidney with two-dimensional and three-dimensional ultrasound. Ultrasound Med Biol 28: 853–858. Chen CP. 2001. Prenatal diagnosis of limb-body wall complex with craniofacial defects, amniotic bands, adhesions and upper limb deficiency. Prenat Diagn 21: 418, 419. Chen ML, Chang CH, Yu CH, Cheng YC, Chang FM. 2001. Prenatal diagnosis of cleft palate by three-dimensional ultrasound. Ultrasound Med Biol 27: 1017–1023. Chmait R, Pretorius D, Jones M, et al. 2002. Prenatal evaluation of facial clefts with two-dimensional and adjunctive three-dimensional ultrasonography: a prospective trial. Am J Obstet Gynecol 187: 946–949. Chuang L, Chang CH, Yu CH, Chang FM. 2000. Three-dimensional sonographic visualization of a fetal omphalocele at 14 weeks of gestation. Prenat Diagn 20: 523, 524. Emanuel PG, Garcia GI, Angtuaco TL. 1995. Prenatal detection of anterior abdominal wall defects with US. Radiographics 15: 517–530. Kang L, Chang CH, Yu CH, Cheng YC, Chang FM. 2002. Prenatal depiction of cystic hygroma using three-dimensional ultrasound. Ultrasound Med Biol 28: 719–723. Lai TH, Chang CH, Yu CH, Kuo PL, Chang FM. 2000. Prenatal diagnosis of alobar holoprosencephaly by two-dimensional and three-dimensional ultrasound. Prenat Diagn 20: 400–403. Sanders RC. 2002. Structural Fetal Abnormalities: The Total Picture (2nd edn), Mosby: St Louis. Wu YC, Yang ML, Yuan CC. 2000. Prenatal diagnosis of anophthalmos with limb-body wall complex. Prenat Diagn 20: 769, 770.

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منابع مشابه

I-44: Increased Nuchal Translucency at 11-14 Weeks of Gestation As A Marker for Adverse Pregnancy Outcomes

Background: To evaluate the association of increased fetal nuchal translucency( NT) and adverse pregnancy outcomes. Materials and Methods: In a prospective study, 2221 women who were conceived after Assisted Conception were investigated by sonography independent of multiplicity between 11 and 13 weeks' gestation. We performed 2899 NT examinations during the study period(21 March 2010 to 21...

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Cerebro-fronto-facial syndrome (Dandy-Walker Variant and frontofacial dysmorphisms): report of the first case identified by increased nuchal translucency beyond 13(+6) weeks.

A 32-year-old gravida 2, para 1 woman, with a previous uneventful pregnancy, underwent first trimester ultrasound screening for Down syndrome at 13 weeks according to the Fetal Medicine Foundation guidelines (http://www.fetalmedicine.com/pdf/11-14/english/FMF-English.pdf). The ultrasound showed increased nuchal translucency (NT) of 8.9 mm with an estimated risk of Down syndrome of 1:8. Fetal ka...

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First-trimester nuchal translucency measurement and echocardiography at 16 to 18 weeks of gestation in prenatal detection for trisomy 18.

BACKGROUND Trisomy 18, the second most common autosomal trisomy, has the highest incidence of congenital heart disease of all chromosomal abnormalities. This study assessed the use of nuchal translucency (NT) measurement and fetal echocardiography at 16 to 18 weeks of gestation in prenatal detection for trisomy 18. METHODS Screening for chromosomal aneuploidy using fetal NT measurement was pe...

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Screening for trisomy 13 by fetal nuchal translucency and maternal serum free beta-hCG and PAPP-A at 10-14 weeks of gestation.

In 42 cases of trisomy 13 at 10-14 weeks of gestation, compared with 947 controls, the median multiple of the median (MoM) of maternal serum free beta-human chorionic gonadotrophin (beta-hCG) and pregnancy associated plasma protein A (PAPP-A) was significantly decreased (0.506 MoM and 0.248 MoM respectively), whilst fetal nuchal translucency was increased (2.872 MoM). In 38% and 71% of cases of...

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Congenital lymphedema presenting with increased nuchal translucency at 13 weeks of gestation.

Congenital lymphedema is an autosomal dominant condition characterized by chronic tissue swelling caused by deficient lymphatic drainage due to hypoplastic/aplastic lymphatic vessels and usually affecting the lower limbs. The locus of the gene has been identified in the long arm of chromosome 15. We report one case of congenital lymphedema presenting with increased nuchal translucency at 13 wee...

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عنوان ژورنال:
  • Prenatal diagnosis

دوره 23 6  شماره 

صفحات  -

تاریخ انتشار 2003