Pre- and postnatal imaging of Pai syndrome with spontaneous intrauterine closure of a frontal cephalocele.
Options
BORIS DOI
Date of Publication
June 2015
Publication Type
Article
Division/Institute
Contributor
Subject(s)
Series
Pediatric radiology
ISSN or ISBN (if monograph)
0301-0449
Publisher
Springer
Language
English
Publisher DOI
PubMed ID
25359433
Description
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.
File(s)
| File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
|---|---|---|---|---|---|---|---|
| art%3A10.1007%2Fs00247-014-3205-8.pdf | text | Adobe PDF | 575.72 KB | published |