A Case of Pai Syndrome: First Reported Case in Korea.
10.14734/kjp.2014.25.1.17
- Author:
Mee HONG
1
;
Seung Woo NAM
;
Yeon Kyung LEE
;
Sun Young KO
;
Son Moon SHIN
Author Information
1. Department of Pediatrics, Cheil General Hospital & Women's Health Care Center, Kwandong University College of Medicine, Seoul, Korea. ykleeped@hanmail.net
- Publication Type:Case Report
- Keywords:
Pai syndrome;
Nasal polyp;
Pericallosal lipoma
- MeSH:
Agenesis of Corpus Callosum;
Alveolar Process;
Cleft Lip;
Korea;
Lipoma;
Nasal Polyps;
Polyps
- From:Korean Journal of Perinatology
2014;25(1):17-21
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Pai syndrome is a rare disorder, first described in 1987. Diagnostic criteria are the presence of the nasal polyp and one of the following: midline cleft lip, congenital polyp of mid-anterior alveolar process, and pericallosal lipoma. Thirty-six cases of Pai syndrome have been described so far. We report 1 case of Pai syndrome accompanied by congenital nasal polyp and callosal lipoma with partial agenesis of corpus callosum, the first time in Korea.
