caa a22 4500 378938134 CHVBK 20180305123645.0 cr unu---uuuuu 161128e20040709xx s 000 0 eng 10.1515/JPM.2004.072 doi (NATIONALLICENCE)gruyter-10.1515/JPM.2004.072 A case report of polysplenia syndrome associated with genital tract duplication anomaly [Elektronische Daten] [N. Engineer, I. Scheimberg, Y. Akinfenwa] Polysplenia syndrome is a condition that persists as a defect of lateralisation, the embryonic process by which the site of body organs is determined. The most frequent manifestations of this syndrome, in addition to polysplenia are complex cardiac malformations, situs inversus, and bilobed lungs. Laterality defects have been known to be due to autosomal recessive inheritance. We report a unique case of polysplenia syndrome in association with genital tract duplication anomaly. Copyright © 2004 by Walter de Gruyter GmbH & Co. KG Human reproduction, growth & development nationallicence Gynaecology & obstetrics nationallicence Paediatric medicine nationallicence Engineer N. aut Scheimberg I. aut Akinfenwa Y. aut Journal of Perinatal Medicine Walter de Gruyter 32/4(2004-07-09), 381-382 0300-5577 32:4<381 2004 32 jpme https://doi.org/10.1515/JPM.2004.072 text/html Onlinezugriff via DOI 1 research article jats NATIONALLICENCE 856 40 https://doi.org/10.1515/JPM.2004.072 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Engineer N. aut NATIONALLICENCE 700 1- Scheimberg I. aut NATIONALLICENCE 700 1- Akinfenwa Y. aut NATIONALLICENCE 773 0- Journal of Perinatal Medicine Walter de Gruyter 32/4(2004-07-09), 381-382 0300-5577 32:4<381 2004 32 jpme CC0 http://creativecommons.org/publicdomain/zero/1.0 nationallicence BK010053 XK010053 XK010000 NATIONALLICENCE NATIONALLICENCE NL-gruyter