Crouzon syndrome associated with acanthosis nigricans: prenatal 2D and 3D ultrasound findings and postnatal 3D CT findings

Crouzon syndrome with acanthosis nigricans (CAN) is a very rare condition with an approximate prevalence of 1 per 1 million newborns. We add the first report on prenatal 2D and 3D ultrasound findings in CAN. In addition we present the postnatal 3D CT findings. The diagnosis was confirmed by molecula...

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Autores principales: Nørgaard, Pernille, Hagen, Casper Petri, Hove, Hanne, Dunø, Morten, Nissen, Kamilla Rothe, Kreiborg, Sven, Jørgensen, Finn Stener
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738349/
https://www.ncbi.nlm.nih.gov/pubmed/23986840
http://dx.doi.org/10.1258/arsr.2012.110017
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author Nørgaard, Pernille
Hagen, Casper Petri
Hove, Hanne
Dunø, Morten
Nissen, Kamilla Rothe
Kreiborg, Sven
Jørgensen, Finn Stener
author_facet Nørgaard, Pernille
Hagen, Casper Petri
Hove, Hanne
Dunø, Morten
Nissen, Kamilla Rothe
Kreiborg, Sven
Jørgensen, Finn Stener
author_sort Nørgaard, Pernille
collection PubMed
description Crouzon syndrome with acanthosis nigricans (CAN) is a very rare condition with an approximate prevalence of 1 per 1 million newborns. We add the first report on prenatal 2D and 3D ultrasound findings in CAN. In addition we present the postnatal 3D CT findings. The diagnosis was confirmed by molecular testing.
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spelling pubmed-37383492013-08-28 Crouzon syndrome associated with acanthosis nigricans: prenatal 2D and 3D ultrasound findings and postnatal 3D CT findings Nørgaard, Pernille Hagen, Casper Petri Hove, Hanne Dunø, Morten Nissen, Kamilla Rothe Kreiborg, Sven Jørgensen, Finn Stener Acta Radiol Short Rep Case Report Crouzon syndrome with acanthosis nigricans (CAN) is a very rare condition with an approximate prevalence of 1 per 1 million newborns. We add the first report on prenatal 2D and 3D ultrasound findings in CAN. In addition we present the postnatal 3D CT findings. The diagnosis was confirmed by molecular testing. SAGE Publications 2012-05-17 /pmc/articles/PMC3738349/ /pubmed/23986840 http://dx.doi.org/10.1258/arsr.2012.110017 Text en © 2012 The Foundation Acta Radiologica http://creativecommons.org/licenses/by-nc/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/2.0/), which permits non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Nørgaard, Pernille
Hagen, Casper Petri
Hove, Hanne
Dunø, Morten
Nissen, Kamilla Rothe
Kreiborg, Sven
Jørgensen, Finn Stener
Crouzon syndrome associated with acanthosis nigricans: prenatal 2D and 3D ultrasound findings and postnatal 3D CT findings
title Crouzon syndrome associated with acanthosis nigricans: prenatal 2D and 3D ultrasound findings and postnatal 3D CT findings
title_full Crouzon syndrome associated with acanthosis nigricans: prenatal 2D and 3D ultrasound findings and postnatal 3D CT findings
title_fullStr Crouzon syndrome associated with acanthosis nigricans: prenatal 2D and 3D ultrasound findings and postnatal 3D CT findings
title_full_unstemmed Crouzon syndrome associated with acanthosis nigricans: prenatal 2D and 3D ultrasound findings and postnatal 3D CT findings
title_short Crouzon syndrome associated with acanthosis nigricans: prenatal 2D and 3D ultrasound findings and postnatal 3D CT findings
title_sort crouzon syndrome associated with acanthosis nigricans: prenatal 2d and 3d ultrasound findings and postnatal 3d ct findings
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738349/
https://www.ncbi.nlm.nih.gov/pubmed/23986840
http://dx.doi.org/10.1258/arsr.2012.110017
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