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Pre- and postnatal imaging of Pai syndrome with spontaneous intrauterine closure of a frontal cephalocele

Dobrocky, Tomas ; Ebner, Lukas ; Liniger, Benjamin ; Weisstanner, Christian ; Stranzinger, Enno

In: Pediatric Radiology, 2015, vol. 45, no. 6, p. 936-940

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    Titel
    • Pre- and postnatal imaging of Pai syndrome with spontaneous intrauterine closure of a frontal cephalocele
    Autor
    • Dobrocky, Tomas. Department of Interventional, Pediatric and Diagnostic Radiology, Inselspital University Hospital, University of Bern, Freiburgstrasse 10, 3010, Bern, Switzerland
    • Ebner, Lukas. Department of Interventional, Pediatric and Diagnostic Radiology, Inselspital University Hospital, University of Bern, Freiburgstrasse 10, 3010, Bern, Switzerland
    • Liniger, Benjamin. Department of Pediatric Surgery, Inselspital University Hospital, University of Bern, Bern, Switzerland
    • Weisstanner, Christian. Department of Diagnostic and Interventional Neuroradiology, Inselspital University Hospital, University of Bern, Bern, Switzerland
    • Stranzinger, Enno. Department of Interventional, Pediatric and Diagnostic Radiology, Inselspital University Hospital, University of Bern, Freiburgstrasse 10, 3010, Bern, Switzerland
    Dokumententyp
    • Postprint
    Sprache
    • Englisch
    Veröffentlicht in
    • Pediatric Radiology, 2015, vol. 45, no. 6, p. 936-940. Springer Berlin Heidelberg
    Andere elektronische Ausgabe
    OAI-PMH-ID
    • oai:doc.rero.ch:331894
    Summary
    Pai syndrome is a rare congenital disorder characterized by cutaneous polyps of the face, pericallosal lipoma and median cleft lip. We report on a newborn girl with a variant of Pai syndrome presenting with all typical findings except a median cleft. In addition, fetal sonography and MRI showed the unique intrauterine evolution of a cephalocele into an atretic cephalocele.