{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T14:25:17Z","timestamp":1786976717198,"version":"build-2736575974"},"reference-count":11,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2005,6,5]],"date-time":"2005-06-05T00:00:00Z","timestamp":1117929600000},"content-version":"vor","delay-in-days":5940,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1989,3]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>The present report describes on a 1\u2010year\u2010old girl with macrocephaly, bulging forehead, ocular hypertelorism, antimongoloid palpebral slant, convergent strabismus, atrophy of optic papillae, short philtrum, protruding lips, high\u2010arched palate, bifid uvula, broad trunk, apparently widely spaced nipples, diastasis recti, small umbilical hernia, tapering fingers, fifth\u2010finger clinodactyly, postaxial polydactyly of the left hand, and bilateral hallux duplication. Partial agenesis of the corpus callosum and central diffuse cortical cerebral atrophy was documented on computed tomography. Chromosomes were normal. Parents were related as half first cousins. Their previous pregnancy had ended in a miscarriage. We suggest that this patient has an acrocallosal syndrome inherited as an autosomal recessive trait. This supports other recent reports that have considered this entity to differ from Greig cephalopolysyndactyly.<\/jats:p>","DOI":"10.1002\/ajmg.1320320303","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T23:28:16Z","timestamp":1118532496000},"page":"298-300","source":"Crossref","is-referenced-by-count":17,"title":["Acrocallosal syndrome in a girl born to consanguineous parents"],"prefix":"10.1002","volume":"32","author":[{"given":"Leonardo J.","family":"Salgado","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carlos A.","family":"Ali","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eduardo E.","family":"Castilla","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,6,5]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320130307"},{"key":"e_1_2_1_3_1","first-page":"403","article-title":"Le syndrome de Greig: Une polysyndactylie variable associee a une dysmorphie craniofaciale distincte","volume":"30","author":"Fryns JP","year":"1982","journal-title":"J G\u00e9n\u00e9t Hum"},{"key":"e_1_2_1_4_1","first-page":"189","article-title":"Oxycephaly","volume":"33","author":"Greig DM","year":"1926","journal-title":"Edinburgh Med J"},{"key":"e_1_2_1_5_1","first-page":"239","article-title":"Schinzel acrocallosal syndrome: A variant example of the Greig syndrome?","volume":"28","author":"Legius E","year":"1985","journal-title":"Ann G\u00e9n\u00e9t"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320120209"},{"key":"e_1_2_1_7_1","first-page":"45","article-title":"Inbreeding in South American newborn series","volume":"6","author":"Orioli IM","year":"1982","journal-title":"Acta Anthropogenet"},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320200115"},{"key":"e_1_2_1_9_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320120210"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1986.tb01897.x"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320060308"},{"key":"e_1_2_1_12_1","doi-asserted-by":"publisher","DOI":"10.1038\/newbio232031a0"}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320320303","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320320303","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,22]],"date-time":"2023-10-22T08:44:59Z","timestamp":1697964299000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320320303"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1989,3]]},"references-count":11,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1989,3]]}},"alternative-id":["10.1002\/ajmg.1320320303"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320320303","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1989,3]]}}}