Mental Development and Surgical Prognosis of Pai Syndrome: A Case Report and Review of the Literature

Cleft Palate Craniofac J. 2019 Feb;56(2):273-279. doi: 10.1177/1055665618771419. Epub 2018 Apr 17.

Abstract

Pai syndrome is a rare congenital disorder, and there are few reports about the long-term prognosis of mental development and surgical results. Here, we report a patient with Pai syndrome who was followed up from birth up to the age of 8 years. Additionally, we review 32 articles and discuss the long-term prognosis of Pai syndrome. In our case, an intracranial lipoma grew a little, but neither epilepsy nor intellectual disabilities occurred. However, she showed attention-deficit/hyperactivity disorder. Furthermore, her nasal airway was gradually obstructed by a residual intranasal polyp.

Keywords: Pai syndrome; long-term follow-up; mental development; prognosis; surgical treatment.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Agenesis of Corpus Callosum
  • Child
  • Cleft Lip
  • Coloboma
  • Female
  • Humans
  • Lipoma*
  • Magnetic Resonance Imaging
  • Nasal Polyps
  • Prognosis
  • Skin Diseases

Supplementary concepts

  • Median cleft lip, corpus callosum, lipoma, and skin polyps