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

Dobrocky, Tomas; Ebner, Lukas Michael; Liniger, Benjamin; Weisstanner, Christian; Stranzinger, Enno (2015). Pre- and postnatal imaging of Pai syndrome with spontaneous intrauterine closure of a frontal cephalocele. Pediatric radiology, 45(6), pp. 936-940. Springer 10.1007/s00247-014-3205-8

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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.

Item Type:

Journal Article (Further Contribution)

Division/Institute:

04 Faculty of Medicine > Department of Radiology, Neuroradiology and Nuclear Medicine (DRNN) > Institute of Diagnostic, Interventional and Paediatric Radiology
04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Paediatric Surgery
04 Faculty of Medicine > Department of Radiology, Neuroradiology and Nuclear Medicine (DRNN) > Institute of Diagnostic and Interventional Neuroradiology

UniBE Contributor:

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

Subjects:

600 Technology > 610 Medicine & health

ISSN:

0301-0449

Publisher:

Springer

Language:

English

Submitter:

Martin Zbinden

Date Deposited:

22 Jan 2015 11:39

Last Modified:

08 Nov 2016 13:15

Publisher DOI:

10.1007/s00247-014-3205-8

PubMed ID:

25359433

BORIS DOI:

10.7892/boris.61853

URI:

https://boris.unibe.ch/id/eprint/61853

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