{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,8]],"date-time":"2025-10-08T22:57:20Z","timestamp":1759964240522,"version":"3.37.3"},"reference-count":11,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2017,8,29]],"date-time":"2017-08-29T00:00:00Z","timestamp":1503964800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Congenital Anomalies"],"published-print":{"date-parts":[[2018,5]]},"abstract":"<jats:title>ABSTRACT<\/jats:title><jats:p>Pallister\u2010<jats:styled-content style=\"fixed-case\">K<\/jats:styled-content>illian syndrome (<jats:styled-content style=\"fixed-case\">PKS<\/jats:styled-content>) is rare genetic disorder caused by tetrasomy 12p mosaicism with supernumerary isochromosome 12p that manifests with intellectual disability, craniofacial dysmorphism, and epilepsy. Although <jats:styled-content style=\"fixed-case\">PKS<\/jats:styled-content> presents as a multisystem morphological defect, respiratory system involvement is rare, except for diaphragmatic hernia. We are the first to report a case of <jats:styled-content style=\"fixed-case\">PKS<\/jats:styled-content> with progressive subglottic stenosis. Subglottic stenosis is a potentially lethal condition due to severe respiratory obstruction and difficult intubation; therefore, further accumulation of cases is required to assess the causal link between <jats:styled-content style=\"fixed-case\">PKS<\/jats:styled-content> and subglottic stenosis.<\/jats:p>","DOI":"10.1111\/cga.12240","type":"journal-article","created":{"date-parts":[[2017,7,26]],"date-time":"2017-07-26T13:06:00Z","timestamp":1501074360000},"page":"102-104","source":"Crossref","is-referenced-by-count":4,"title":["Progressive subglottic stenosis in a child with <scp>P<\/scp>allister\u2010<scp>K<\/scp>illian syndrome"],"prefix":"10.1111","volume":"58","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-0076-5882","authenticated-orcid":false,"given":"Tadashi","family":"Shiohama","sequence":"first","affiliation":[{"name":"Department of Pediatrics Chiba University Graduate School of Medicine  Chiba Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Katsunori","family":"Fujii","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Chiba University Graduate School of Medicine  Chiba Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kenji","family":"Shimizu","sequence":"additional","affiliation":[{"name":"Divsion of Medical Genetics Saitama Children's Medical Center  Saitama Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hirofumi","family":"Ohashi","sequence":"additional","affiliation":[{"name":"Divsion of Medical Genetics Saitama Children's Medical Center  Saitama Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tomozumi","family":"Takatani","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Chiba University Graduate School of Medicine  Chiba 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