Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tascha Gehrke"'
Autor:
Ivonne Alexandra Bedei, Alexander Graf, Karl-Philipp Gloning, Matthias Meyer-Wittkopf, Daria Willner, Martin Krapp, Sabine Hentze, Alexander Scharf, Jan Degenhardt, Kai-Sven Heling, Peter Kozlowski, Kathrin Trautmann, Kai Jahns, Anne Geipel, Ismail Tekesin, Michael Elsässer, Lucas Wilhelm, Ingo Gottschalk, Jan-Erik Baumüller, Cahit Birdir, Felix Zöllner, Aline Wolter, Johanna Schenk, Tascha Gehrke, Corinna Keil, Jimmy Espinosa, Roland Axt-Fliedner
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 15, p 4588 (2022)
Mirror syndrome is a rare and serious maternal condition associated with immune and non-immune fetal hydrops after 16 weeks of gestational age. Subjacent conditions associated with fetal hydrops may carry different risks for Mirror syndrome. Fetuses
Externí odkaz:
https://doaj.org/article/dce3865ca0ca4bfbac29baf71a546159
Autor:
Ivonne Bedei, Karl‐Philipp Gloning, Luc Joyeux, Matthias Meyer‐Wittkopf, Daria Willner, Martin Krapp, Alexander Scharf, Jan Degenhardt, Kai‐Sven Heling, Peter Kozlowski, Kathrin Trautmann, Kai M. Jahns, Annegret Geipel, Ismail Tekesin, Michael Elsässer, Lucas Wilhelm, Ingo Gottschalk, Jan‐Erik Baumüller, Cahit Birdir, Andreas Schröer, Felix Zöllner, Aline Wolter, Johanna Schenk, Tascha Gehrke, Alicia Spaeth, Roland Axt‐Fliedner
Publikováno v:
Prenatal Diagnosis. 43:183-191
Autor:
Ivonne, Bedei, Karl-Philipp, Gloning, Joyeux, Luc, Matthias, Meyer-Wittkopf, Daria, Willner, Martin, Krapp, Alexander, Scharf, Jan, Degenhardt, Kai-Sven, Heling, Peter, Kozlowski, Kathrin, Trautmann, Kai M, Jahns, Annegret, Geipel, Ismail, Tekesin, Michael, Elsässer, Lucas, Wilhelm, Ingo, Gottschalk, Jan-Erik, Baumüller, Cahit, Birdir, Andreas, Schröer, Felix, Zöllner, Aline, Wolter, Johanna, Schenk, Tascha, Gehrke, Alicia, Spaeth, Roland, Axt-Fliedner
Publikováno v:
Prenatal diagnosis.
Omphalocele is known to be associated with genetic anomalies like trisomy 13, 18 and Beckwith-Wiedemann syndrome, but not with Turner syndrome (TS). Our aim was to assess the incidence of omphalocele in fetuses with TS, the phenotype of this associat