Phenotypic variability of Pai syndrome: report of two patients and review of the literature

Int J Oral Maxillofac Surg. 2008 Nov;37(11):1059-64. doi: 10.1016/j.ijom.2008.06.007. Epub 2008 Jul 25.

Abstract

Pai syndrome is a rare form of frontonasal dysplasia, first described in 1987. It is a triad consisting of midline cleft of the upper lip, facial skin polyps and central nervous system lipomas. Only 14 cases have been reported in the literature. The authors describe the clinical features, diagnostic workup and treatment of two patients. A review of all cases reported in literature is presented to show the phenotypic variability of this rare syndrome.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Abnormalities, Multiple / surgery*
  • Bone Diseases, Developmental / complications
  • Bone Diseases, Developmental / surgery*
  • Child, Preschool
  • Cleft Lip / complications
  • Cleft Lip / surgery*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Labial Frenum / abnormalities
  • Labial Frenum / surgery
  • Nasal Cartilages / abnormalities*
  • Nasal Cartilages / surgery
  • Nasal Polyps / complications
  • Nasal Polyps / surgery*
  • Nasal Septum / abnormalities*
  • Nasal Septum / surgery
  • Nose / abnormalities
  • Nose / surgery
  • Syndrome
  • Treatment Outcome