Literature DB >> 25359433

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

Tomas Dobrocky1, Lukas Ebner, Benjamin Liniger, Christian Weisstanner, Enno Stranzinger.   

Abstract

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.

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Mesh：

Year:  2014        PMID： 25359433     DOI： 10.1007/s00247-014-3205-8

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN： 0301-0449


  8 in total

Review 1.  Atypical findings in three patients with Pai syndrome and literature review.

Authors:  Damien Lederer; Brian Wilson; Pierre Lefesvre; Vincent Vander Poorten; Nigel Kirkham; Dipayan Mitra; Christine Verellen-Dumoulin; Koenraad Devriendt
Journal:  Am J Med Genet A       Date:  2012-09-17       Impact factor: 2.802

2.  Geographical distribution of fronto-ethmoidal encephalomeningocele.

Authors:  C Suwanwela
Journal:  Br J Prev Soc Med       Date:  1972-08

3.  An unusual case of cephalocele associated with lipoma of corpus callosum.

Authors:  R Ergün; A I Okten; U Bostanci
Journal:  Pediatr Neurosurg       Date:  1999-01       Impact factor: 1.162

Review 4.  Pai syndrome (median cleft palate, cutaneous nasal polyp, and midline lipoma of the corpus callosum): a case report and literature review.

Authors:  Chris Szeto; Ted L Tewfik; David Jewer; Arthur Rideout
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2005-09       Impact factor: 1.675

5.  Prenatal diagnosis and postnatal follow-up of pericallosal lipoma: report of seven new cases.

Authors:  V Ickowitz; D Eurin; F Rypens; P Sonigo; I Simon; P David; F Brunelle; F E Avni
Journal:  AJNR Am J Neuroradiol       Date:  2001-04       Impact factor: 3.825

6.  Median cleft of the upper lip associated with lipomas of the central nervous system and cutaneous polyps.

Authors:  G S Pai; A H Levkoff; R E Leithiser
Journal:  Am J Med Genet       Date:  1987-04

7.  Pai syndrome: challenging prenatal diagnosis and management.

Authors:  Marie Blouet; Frédérique Belloy; Corinne Jeanne-Pasquier; Nathalie Leporrier; Guillaume Benoist
Journal:  Pediatr Radiol       Date:  2014-04-20

8.  Spontaneous regression of lipomyelomeningocele associated with terminal syringomyelia in a child. Case report.

Authors:  Olivier Klein; Dominic Thompson
Journal:  J Neurosurg       Date:  2007-09       Impact factor: 5.115
  8 in total
  4 in total

1.  Atretic cephaloceles: a comprehensive analysis of historical cohort.

Authors:  Mustafa Kemal Demir; Ahmet Çolak; Murat Şakir Ekşi; Emel Ece Özcan-Ekşi; Akın Akakın; Baran Yılmaz
Journal:  Childs Nerv Syst       Date:  2016-07-26       Impact factor: 1.475

Review 2.  Pai syndrome: a review.

Authors:  Francesca Olivero; Thomas Foiadelli; Sabino Luzzi; Gian Luigi Marseglia; Salvatore Savasta
Journal:  Childs Nerv Syst       Date:  2020-07-10       Impact factor: 1.475

3.  Pai syndrome: From the womb until 19 months of age, a neurological development success story.

Authors:  Hala Hassan; Daniella L Buzas; Anne Bazin; Noëlle Stempfle; Agnès Guët; Christophe Poncelet; Cergika Veluppillai
Journal:  Clin Case Rep       Date:  2021-07-21

Review 4.  The spectrum of venous anomalies associated with atretic parietal cephaloceles: A literature review.

Authors:  Serra Sencer; Mohamed M Arnaout; Hosam Al-Jehani; Zahraa A Alsubaihawi; Zahraa F Al-Sharshahi; Samer S Hoz
Journal:  Surg Neurol Int       Date:  2021-07-06
  4 in total

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