Fetal MRI of the heart and brain in congenital heart disease

Autor: Anouk S Moerdijk, Nathalie HP Claessens, Inge M van Ooijen, Pim van Ooij, Thomas Alderliesten, Heynric B Grotenhuis, MN Bekker, MJNL Benders, AE Bohte, JMPJ Breur, D Charisopoulou, S-A Clur, JMJ Cornette, Z Fejzic, MTM Franssen, S Frerich, LM Geerdink, ATJI Go, S Gommers, WA Helbing, A Hirsch, RJ Holtackers, WM Klein, GJ Krings, HJ Lamb, M Nijman, E Pajkrt, RN Planken, EM Schrauben, TJ Steenhuis, H ter Heide, WYR Vanagt, IM van Beynum, MD van Gaalen, GG van Iperen, J van Schuppen, TP Willems, I Witters

Publikováno v: The Lancet Child & Adolescent Health, 7, 1, pp. 59-68
FUTURE 2.0 consortium 2023, ' Fetal MRI of the heart and brain in congenital heart disease ', The Lancet Child and Adolescent Health, vol. 7, no. 1, pp. 59-68 . https://doi.org/10.1016/S2352-4642(22)00249-8
The Lancet Child & Adolescent Health, 7, 59-68

Item does not contain fulltext Antenatal assessment of congenital heart disease and associated anomalies by ultrasound has improved perinatal care. Fetal cardiovascular MRI and fetal brain MRI are rapidly evolving for fetal diagnostic testing of cong

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7732cea40b5a5d7bd482caf9eb066b8
https://pubmed.ncbi.nlm.nih.gov/36343660

EP04.12: Perinatal features of Smith‐Lemli‐Opitz Syndrome

Autor: Y. Arens, R. Bernaerts, I. Witters, A. Coumans

Publikováno v: Ultrasound in Obstetrics & Gynecology. 54:251-252

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ff13ff20cc4496da0a52df7010615dcb
https://doi.org/10.1002/uog.21167

Prenatal Diagnosis of the Wolf-Hirschhorn Syndrome with Increased Nuchal Translucency and Negative Serum Integrated Screening for Trisomy 21

Autor: Soetinah Wirjosoekarto, Jean-Pierre Fryns, A. Coumans, Wilfried Gyselaers, Christine Willekes, Paul Viaene, Tine Mesens, I Witters

Publikováno v: Ultrasound. 19:224-226

The Wolf-Hirschhorn syndrome (WHS) is a contiguous gene deletion syndrome associated with a hemizygous deletion of chromosome 4p16.3. It is characterized by pre- and postnatal growth restriction, microcephaly, profound learning disability and seizure

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8775bcb5071680fdb4f27bbadee24b53
https://doi.org/10.1258/ult.2011.011023

Pericardial effusion in the first trimester of pregnancy

Autor: Claire Theyskens, Luc De Catte, Marc Gewillig, Els Bruneel, Wilfried Gyselaers, Derize Boshoff, Jean-Pierre Fryns, I Witters, Tinne Mesens

Publikováno v: Prenatal Diagnosis. 31:215-217

Ingrid Witters1,2,6*, Derize Boshoff3, Luc De Catte4, Tinne Mesens2, Wilfried Gyselaers2, Claire Theyskens2, Els Bruneel2, Marc Gewillig5 and Jean-Pierre Fryns1 1Center for Human Genetics, Catholic University of Leuven, Leuven, Belgium 2Department of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a64a29f1d6e136c8fa01db037254a5c3
https://doi.org/10.1002/pd.2667

Congenital High Airway Obstruction Syndrome (CHAOS) as part of Fraser syndrome: ultrasound and autopsy findings

Autor: T, Mesens, I, Witters, J, Van Robaeys, H, Peeters, J P, Fryns

Publikováno v: Genetic counseling (Geneva, Switzerland). 24(4)

Congenital High Airway Obstruction Syndrome (CHAOS) is a potential lethal condition. We describe a case report of CHAOS, with additional malformations diagnosed at 20 weeks. Autopsy findings are suggestive for Fraser syndrome (cryptophthalmos-syndact

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a006445819996368039f8c45aef724ed
https://pubmed.ncbi.nlm.nih.gov/24551978