{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T21:17:28Z","timestamp":1790457448613,"version":"4.1.0"},"reference-count":10,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2018,4,15]],"date-time":"2018-04-15T00:00:00Z","timestamp":1523750400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["obgyn.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Prenatal Diagnosis"],"published-print":{"date-parts":[[2018,5]]},"abstract":"<jats:p>What's already known about the topic?\n<jats:list list-type=\"bullet\">\n<jats:list-item><jats:p>Proteus syndrome is a rare condition characterized by mosaic overgrowth of tissue types derived from all 3 germ layers. It has a highly variable presentation and is generally diagnosed by clinical criteria after birth.<\/jats:p><\/jats:list-item>\n<\/jats:list><\/jats:p><jats:p>What does this study add?\n<jats:list list-type=\"bullet\">\n<jats:list-item><jats:p>This case describes the ultrasound and autopsy findings of a rare presentation of a fetus with AKT1\u2010related Proteus syndrome.<\/jats:p><\/jats:list-item>\n<jats:list-item><jats:p>It demonstrates many systemic and neurologic findings of Proteus syndrome in a fetus that have not been reported in the literature.<\/jats:p><\/jats:list-item>\n<jats:list-item><jats:p>Prenatal diagnosis of mutant AKT1\u2010related Proteus syndrome by antenatal ultrasound is possible and may present without obvious segmentation in a severe phenotype.<\/jats:p><\/jats:list-item>\n<\/jats:list><\/jats:p>","DOI":"10.1002\/pd.5252","type":"journal-article","created":{"date-parts":[[2018,3,25]],"date-time":"2018-03-25T12:44:20Z","timestamp":1521981860000},"page":"467-470","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":6,"title":["Prenatal diagnosis of a fetus with Proteus syndrome"],"prefix":"10.1002","volume":"38","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-1615-180X","authenticated-orcid":false,"given":"Lauren","family":"Fogarty","sequence":"first","affiliation":[{"name":"Dalhousie Medical School  Halifax Nova Scotia Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lauren","family":"Currie","sequence":"additional","affiliation":[{"name":"Maritime Medical Genetics Service, IWK Health Centre  Halifax Nova Scotia 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