{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T10:53:29Z","timestamp":1790420009097,"version":"4.1.0"},"reference-count":23,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2017,11,28]],"date-time":"2017-11-28T00:00:00Z","timestamp":1511827200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100001665","name":"ANR","doi-asserted-by":"publisher","award":["2013 CILAXCAL, ANR\u201013\u2010BSV1\u20100027"],"award-info":[{"award-number":["2013 CILAXCAL, ANR\u201013\u2010BSV1\u20100027"]}],"id":[{"id":"10.13039\/501100001665","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100006005","name":"Agence de la Biom\u00e9decine","doi-asserted-by":"publisher","award":["AOR 2010"],"award-info":[{"award-number":["AOR 2010"]}],"id":[{"id":"10.13039\/501100006005","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001665","name":"Agence Nationale de la Recherche","doi-asserted-by":"publisher","award":["ANR\u2010A0\u2010IAHU\u201001"],"award-info":[{"award-number":["ANR\u2010A0\u2010IAHU\u201001"]}],"id":[{"id":"10.13039\/501100001665","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100002915","name":"Fondation pour la Recherche M\u00e9dicale","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100002915","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Birth Defects Research"],"published-print":{"date-parts":[[2018,3]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p>OFD1 syndrome is a rare ciliopathy inherited on a dominant X\u2010linked mode, typically lethal in males in the first or second trimester of pregnancy. It is characterized by oral cavity and digital anomalies possibly associated with cerebral and renal signs. Its prevalence is between 1\/250,000 and 1\/50,000 births. It is due to heterozygous mutations of <jats:italic>OFD1<\/jats:italic> and mutations are often de novo (75%). Familial forms show highly variable phenotypic expression. <jats:italic>OFD1<\/jats:italic> encodes a protein involved in centriole growth, distal appendix formation, and ciliogenesis.<\/jats:p><\/jats:sec><jats:sec><jats:title>Cases<\/jats:title><jats:p>We report the investigation of three female fetuses in which corpus callosum agenesis was detected by ultrasound during the second trimester of pregnancy. In all three fetuses, fetopathological examination allowed the diagnosis of OFD1 syndrome, which was confirmed by molecular analysis.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>To our knowledge, these are the first case reports of antenatal diagnosis of OFD1 syndrome in the absence of familial history, revealed following detection of agenesis of the corpus callosum. They highlight the impact of fetal examination following termination of pregnancy for brain malformations. They also highlight the contribution of ciliary genes to corpus callosum development.<\/jats:p><\/jats:sec>","DOI":"10.1002\/bdr2.1154","type":"journal-article","created":{"date-parts":[[2017,11,29]],"date-time":"2017-11-29T15:19:30Z","timestamp":1511968770000},"page":"382-389","source":"Crossref","is-referenced-by-count":10,"title":["In utero ultrasound diagnosis of corpus callosum agenesis leading to the identification of orofaciodigital type 1 syndrome in female fetuses"],"prefix":"10.1002","volume":"110","author":[{"given":"Caroline","family":"Alby","sequence":"first","affiliation":[{"name":"INSERM U1163, Institut Imagine Universit\u00e9 Paris Descartes Paris France"},{"name":"Unit\u00e9 d'Embryofoetopathologie, Service d'Histologie\u2010Embryologie\u2010Cytog\u00e9n\u00e9tique H\u00f4pital Necker\u2010Enfants Malades, APHP Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lucile","family":"Boutaud","sequence":"additional","affiliation":[{"name":"INSERM 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