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


Autoria(s): Dobrocky, Tomas; Ebner, Lukas Michael; Liniger, Benjamin; Weisstanner, Christian; Stranzinger, Enno
Data(s)

01/06/2015

Resumo

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.

Formato

application/pdf

Identificador

http://boris.unibe.ch/61853/1/art%253A10.1007%252Fs00247-014-3205-8.pdf

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 <http://dx.doi.org/10.1007/s00247-014-3205-8>

doi:10.7892/boris.61853

info:doi:10.1007/s00247-014-3205-8

info:pmid:25359433

urn:issn:0301-0449

Idioma(s)

eng

Publicador

Springer

Relação

http://boris.unibe.ch/61853/

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

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 <http://dx.doi.org/10.1007/s00247-014-3205-8>

Palavras-Chave #610 Medicine & health
Tipo

info:eu-repo/semantics/article

info:eu-repo/semantics/publishedVersion

PeerReviewed