| Literature DB >> 22987662 |
Damien Lederer1, Brian Wilson, Pierre Lefesvre, Vincent Vander Poorten, Nigel Kirkham, Dipayan Mitra, Christine Verellen-Dumoulin, Koenraad Devriendt.
Abstract
Pai syndrome is a rare disorder characterized by congenital nasal or facial polyp, midline cleft lip, pericallosal lipoma, ocular anomalies, and normal neuropsychological development. Here, we report on three patients with Pai syndrome and atypical findings: temporal triangular alopecia, posterior lenticonus, bilateral palatal pits, bifid uvula, hypospadias, sacral dimple, true tracheal bronchus, and epilepsy. Thirty-three cases of Pai syndrome have been described so far. We present a review of the previously reported cases and suggest modified diagnostic criteria for Pai syndrome.Entities:
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Year: 2012 PMID: 22987662 DOI: 10.1002/ajmg.a.35592
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802