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Number of results

Journal

2013 | 8 | 4 | 431-433

Article title

Prenatally diagnosed fetal omphalocele at 11 week gestation - a case report

Content

Title variants

Languages of publication

EN

Abstracts

EN
Omphalocele is the most common congenital defect of the abdominal wall and in a large percentage of cases it is associated with chromosomal anomalies. In this case report during the regular ultrasound examination at 11 weeks of gestation, omphalocela, whose scope was 90% of fetal abdomen, was diagnosed. Karyotype analysis showed the presence of chromosomal aberrations 47 XX + 18 (Edwards syndrome). After the presentation of the severity of congenital anomalies and characteristic of the Edwards syndrome patient decided to terminate the pregnancy.

Keywords

Publisher

Journal

Year

Volume

8

Issue

4

Pages

431-433

Physical description

Dates

published
1 - 8 - 2013
online
12 - 6 - 2013

Contributors

author
  • Department of Gynecology and Obstretic, Clinical Center Kragujevac, 30 Zmaj Jovina Str., 34000, Kragujevac, Serbia
  • Department of Gynecology and Obstretic, Clinical Center Kragujevac, 30 Zmaj Jovina Str., 34000, Kragujevac, Serbia
  • Department of Gynecology and Obstretic, Clinical Center Kragujevac, 30 Zmaj Jovina Str., 34000, Kragujevac, Serbia
author
  • Department of Gynecology and Obstretic, Clinical Center Kragujevac, 30 Zmaj Jovina Str., 34000, Kragujevac, Serbia
  • Department of Gynecology and Obstretic, Clinical Center Kragujevac, 30 Zmaj Jovina Str., 34000, Kragujevac, Serbia
  • Department of Gynecology and Obstretic, Clinical Center Kragujevac, 30 Zmaj Jovina Str., 34000, Kragujevac, Serbia
  • Department of Pathology, Clinical Center Kragujevac, 30 Zmaj Jovina Str., 34000, Kragujevac, Serbia

References

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  • [4] Hsu C.C., Lin S.P., Chen C.H., Chi C.S., Lee H.C., Hung H.Y., et al., Omphalocele and gastroschisis in Taiwan, Eur. J. Pediatr., 2002, 161, 552–555 http://dx.doi.org/10.1007/s00431-002-1031-8[Crossref]
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  • [6] Nicolaides K.H., Snijders R.J., Cheng H.H., Gosden C., Fetal gastro-intestinal and abdominal wall defects: associated malformations and chromosomal abnormalities, Fetal. Diagn. Ther., 1992, 7, 102–115 http://dx.doi.org/10.1159/000263657[Crossref]
  • [7] Smigiel R., Jakubiak A., Lombardi M.P., Jaworski W., Slezak R., Patkowski D., et al., Co-occurrence of severe Goltz-Gorlin syndrome and pentalogy of Cantrell - Case report and review of the literature, Am. J. Med. Genet. A., 2011, 155, 1102–1105 http://dx.doi.org/10.1002/ajmg.a.33895[WoS][Crossref]
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  • [10] Chen C.P., Prenatal sonographic features of fetuses in trisomy 13 pregnancies (III), Taiwan J. Obstet. Gynecol., 2009, 48, 342–349 http://dx.doi.org/10.1016/S1028-4559(09)60322-3[Crossref]
  • [11] Sepulveda W., Wong A.E., Dezerega V., First-trimester sonographic findings in trisomy 18: a review of 53 cases, Prenat. Diagn., 2010, 30, 256–259
  • [12] Getachew M.M., Goldstien R.B., Edge V., Correlation between omphalocele contents and karyotypic abnormalities: Sonographic study in 37 cases, AJR, 1992, 158, 133–136 http://dx.doi.org/10.2214/ajr.158.1.1727339[Crossref]
  • [13] De Veciana M., Major C.A., Porto M., Prediction of an abnormal karyotipe in fetusis with omphalocele, Prenat. Diag., 1994, 14, 487–492 http://dx.doi.org/10.1002/pd.1970140613[Crossref]
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Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_s11536-012-0134-5
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