Literature DB >> 23610859

Prenatal detection of Pai syndrome without cleft lip and palate: a case report.

Z Ocak1, H F Yazicioglu, M Aygun, M K I Ilter, T Ozlu.   

Abstract

Pai syndrome is a rarely encountered disease characterized by findings of median cleft lip, facial skin polyps, nasal mucosal polyps and midline central nervous system lipoma. We report a case with prenatal detection of a pericallosal lipoma and a skin tag on the forehead. After delivery, the diagnosis was confirmed as a case of Pai syndrome.

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Year:  2013        PMID: 23610859

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  2 in total

1.  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

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

  2 in total

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