{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,5]],"date-time":"2026-01-05T15:04:39Z","timestamp":1767625479591,"version":"3.48.0"},"reference-count":18,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2025,8,12]],"date-time":"2025-08-12T00:00:00Z","timestamp":1754956800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100021171","name":"Basic and Applied Basic Research Foundation of Guangdong Province","doi-asserted-by":"publisher","award":["2021A1515220106"],"award-info":[{"award-number":["2021A1515220106"]}],"id":[{"id":"10.13039\/501100021171","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J of Clinical Ultrasound"],"published-print":{"date-parts":[[2026,1]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>X\u2010linked hypohidrotic ectodermal dysplasia (HED) is a rare congenital hereditary disorder primarily affecting ectodermal\u2010derived organs, including hair, sweat glands, and teeth. This case report presents a prenatal diagnosis of HED in a fetus without a familial history or parental phenotypic manifestations. The critical prenatal ultrasound finding was an abnormality in the alveolar bone. Genetic testing confirmed the fetus as a hemizygote for a mutation in the ectodysplasin A gene. This comprehensive study delineates the prenatal ultrasound observations, genetic testing outcomes, and post\u2010mortem pathological findings associated with this syndrome. We also highlight essential considerations for early diagnosis through prenatal ultrasound examinations.<\/jats:p>","DOI":"10.1002\/jcu.70033","type":"journal-article","created":{"date-parts":[[2025,8,13]],"date-time":"2025-08-13T03:39:22Z","timestamp":1755056362000},"page":"229-233","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Prenatal Ultrasound Findings of X\u2010Linked Hypohidrotic Ectodermal Dysplasia: A Case Report"],"prefix":"10.1002","volume":"54","author":[{"given":"Lingna","family":"She","sequence":"first","affiliation":[{"name":"Department of Ultrasound, Meizhou People's Hospital Meizhou Academy of Medical Sciences  Meizhou China"},{"name":"Department of Prenatal Diagnostic Center, Meizhou People's Hospital Meizhou Academy of Medical Sciences  Meizhou China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Man","family":"Yang","sequence":"additional","affiliation":[{"name":"Department 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