| Literature DB >> 29665340 |
Yoshimichi Imai1, Shigeo Kure2, Chieko Nara2, Naoyuki Takagi1, Masahiro Tachi1.
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.Entities:
Keywords: Pai syndrome; long-term follow-up; mental development; prognosis; surgical treatment
Year: 2018 PMID: 29665340 DOI: 10.1177/1055665618771419
Source DB: PubMed Journal: Cleft Palate Craniofac J ISSN: 1055-6656