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Neuronal heterotopias were present in five patients and parieto\u2010occipital encephalocele in three patients. We suggest that this pattern found exclusively in males, most likely represents a newly recognized syndrome distilled from the group of disorders subsumed under frontonasal dysplasia. \u00a9 2009 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.32717","type":"journal-article","created":{"date-parts":[[2009,4,13]],"date-time":"2009-04-13T18:18:57Z","timestamp":1239646737000},"page":"1006-1011","source":"Crossref","is-referenced-by-count":18,"title":["Frontonasal dysplasia, severe neuropsychological delay, and midline central nervous system anomalies: Report of 10 Brazilian male patients"],"prefix":"10.1002","volume":"149A","author":[{"given":"Maria Leine","family":"Guion\u2010Almeida","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Antonio","family":"Richieri\u2010Costa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2009,4,23]]},"reference":[{"key":"e_1_2_5_2_1","first-page":"85","article-title":"Craniofrontonasal dysplasia","volume":"15","author":"Cohen MM","year":"1979","journal-title":"Birth Defects"},{"key":"e_1_2_5_3_1","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.17.10.961"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1590\/S0004-282X2004000200001"},{"key":"e_1_2_5_5_1","first-page":"183","article-title":"A new syndrome of oculoauriculovertebral dysplasia and midline craniofacial defect: The oculoauriculofrontonasal syndrome. 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