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Method of Studying Palatal Fusion using Static Organ Culture
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Prenatal detection of Pai syndrome without cleft lip and palate: a case report
Z Ocak1, H F Yazicioglu, M Aygun
1Department of Medical Genetics, Suleymaniye Maternity Hospital for Research and Training, Istanbul, Turkey. zeynep_ipek@yahoo.com
Abstract:
Pai syndrome is a rarely encountered disease characterized by findings of median cleft lip, facial skin polyps, nasal mucosal polyps and midline central nervous system lipoma. We report a case with prenatal detection of a pericallosal lipoma and a skin tag on the forehead. After delivery, the diagnosis was confirmed as a case of Pai syndrome.
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