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

Authors
Journal
International Journal of Pediatric Otorhinolaryngology
0165-5876
Publisher
Elsevier
Publication Date
Volume
69
Issue
9
Identifiers
DOI: 10.1016/j.ijporl.2005.01.038
Keywords
  • Pai Syndrome
  • Median Cleft Palate
  • Nasal Polyp
  • Lipoma Of Corpus Callosum

Abstract

Summary In this article, we describe a patient with Pai syndrome. This infant was born with an unusual median cleft of the upper lip, a pedunculated cutaneous mass that protruded from the right nostril, double frenulum of the upper lip, and median alveolar cleft. MRI showed a midline corpus callosal lipoma. Mental development was normal and chromosomal analysis revealed a normal male 46, XY karyotype.

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