{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T17:36:18Z","timestamp":1791999378816,"version":"4.4.0"},"reference-count":21,"publisher":"BMJ","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1994,2]]},"abstract":"<jats:p>We present an infant with true trisomy 22. Mosaicism is ruled out by the finding of a 47,XX, +22 karyotype in all cells analysed originating from two embryonic germ layers. The physical findings are consistent with the previously noted features including developmental delay, ear abnormalities, micrognathia, clefting, and congenital heart disease. The patient is the first described with macrocephaly and hydrocephalus and the second with holoprosencephaly.<\/jats:p>","DOI":"10.1136\/jmg.31.2.141","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:23:16Z","timestamp":1226330596000},"page":"141-144","source":"Crossref","is-referenced-by-count":12,"title":["Hydrocephalus in an infant with trisomy 22."],"prefix":"10.1136","volume":"31","author":[{"given":"F","family":"Fahmi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S","family":"Schmerler","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R G","family":"Hutcheon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[1994,2,1]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1136\/jmg.24.2.65","article-title":"Human chromosome 22","volume":"24","author":"Kaplan, J.; Aurias, A.; Julier, C.; Prieur, M.; Szajnert, M.","year":"1987","unstructured":"Kaplan J, Aurias A, Julier C, Prieur M, Szajnert M. 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