{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:18:41Z","timestamp":1787015921970,"version":"build-2736575974"},"reference-count":7,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2016,7,28]],"date-time":"2016-07-28T00:00:00Z","timestamp":1469664000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatric Dermatology"],"published-print":{"date-parts":[[2016,9]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    Acro\u2010dermato\u2010ungual\u2010lacrimal\u2010tooth (\n                    <jats:styled-content style=\"fixed-case\">ADULT<\/jats:styled-content>\n                    ) syndrome is a rare form of autosomal dominant ectodermal dysplasia due to mutations in the\n                    <jats:italic>\n                      <jats:styled-content style=\"fixed-case\">TP<\/jats:styled-content>\n                      63\n                    <\/jats:italic>\n                    gene, a locus that has also been implicated in other syndromic forms of ectodermal dysplasia. It shares many phenotypic characteristics with other\n                    <jats:italic>\n                      <jats:styled-content style=\"fixed-case\">TP<\/jats:styled-content>\n                      63\n                    <\/jats:italic>\n                    gene mutation syndromes, often making an accurate diagnosis difficult. Long\u2010term management and follow\u2010up of the various sequelae of ectodermal dysplasia require an accurate diagnosis. We report a familial case of\n                    <jats:styled-content style=\"fixed-case\">ADULT<\/jats:styled-content>\n                    syndrome in a daughter, mother, and son and provide a brief review of the clinical characteristics of this syndrome.\n                  <\/jats:p>","DOI":"10.1111\/pde.12938","type":"journal-article","created":{"date-parts":[[2016,9,6]],"date-time":"2016-09-06T00:27:33Z","timestamp":1473121653000},"source":"Crossref","is-referenced-by-count":8,"title":["Acro\u2010Dermato\u2010Ungual\u2010Lacrimal\u2010Tooth Syndrome: An Uncommon Member of the Ectodermal Dysplasias"],"prefix":"10.1111","volume":"33","author":[{"given":"Adam","family":"Whittington","sequence":"first","affiliation":[{"name":"Division of Dermatology Ann and Robert H. Lurie Children's Hospital of Chicago Northwestern University Chicago Illinois"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sarah","family":"Stein","sequence":"additional","affiliation":[{"name":"Section of Dermatology University of Chicago Chicago Illinois"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brandi","family":"Kenner\u2010Bell","sequence":"additional","affiliation":[{"name":"Division of Dermatology Ann and Robert H. Lurie Children's Hospital of Chicago Northwestern University Chicago Illinois"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2016,7,28]]},"reference":[{"key":"e_1_2_4_2_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.39.6.377"},{"key":"e_1_2_4_3_1","doi-asserted-by":"publisher","DOI":"10.1086\/323123"},{"key":"e_1_2_4_4_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320450525"},{"key":"e_1_2_4_5_1","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/11.7.799"},{"key":"e_1_2_4_6_1","doi-asserted-by":"publisher","DOI":"10.1111\/bjd.13159"},{"key":"e_1_2_4_7_1","volume-title":"Online Mendelian Inheritance in Man","author":"Hamosh DA","year":"2014"},{"key":"e_1_2_4_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/B978-1-4377-0412-9.00007-1"}],"container-title":["Pediatric Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fpde.12938","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/pde.12938","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,23]],"date-time":"2023-09-23T21:07:46Z","timestamp":1695503266000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/pde.12938"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,7,28]]},"references-count":7,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2016,9]]}},"alternative-id":["10.1111\/pde.12938"],"URL":"https:\/\/doi.org\/10.1111\/pde.12938","archive":["Portico"],"relation":{},"ISSN":["0736-8046","1525-1470"],"issn-type":[{"value":"0736-8046","type":"print"},{"value":"1525-1470","type":"electronic"}],"subject":[],"published":{"date-parts":[[2016,7,28]]}}}