{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,27]],"date-time":"2025-09-27T13:49:40Z","timestamp":1758980980528},"reference-count":15,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2016,7,14]],"date-time":"2016-07-14T00:00:00Z","timestamp":1468454400000},"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><jats:p>Incontinentia pigmenti (<jats:styled-content style=\"fixed-case\">IP<\/jats:styled-content>) is an X\u2010linked dominant disorder that in most cases is considered lethal in males. <jats:styled-content style=\"fixed-case\">IP<\/jats:styled-content> affects the skin, hair, teeth, nails, eyes, and central nervous system. We report a case of persistent hypercalcemia (10.6\u201311.3 mg\/<jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>) in a 19\u2010month\u2010old Caucasian boy with clinical <jats:styled-content style=\"fixed-case\">IP<\/jats:styled-content>. The proposed mechanism for his hypercalcemia is discussed.<\/jats:p>","DOI":"10.1111\/pde.12925","type":"journal-article","created":{"date-parts":[[2016,7,14]],"date-time":"2016-07-14T10:31:14Z","timestamp":1468492274000},"source":"Crossref","is-referenced-by-count":3,"title":["Incontinentia Pigmenti with Persistent Hypercalcemia: Case Report"],"prefix":"10.1111","volume":"33","author":[{"given":"Jacob","family":"Adashek","sequence":"first","affiliation":[{"name":"College of Osteopathic Medicine of the Pacific Western University of Health Sciences Pomona California"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Weiyi","family":"Mu","sequence":"additional","affiliation":[{"name":"McKusick\u2010Nathans Institute of Genetic Medicine Johns Hopkins University Baltimore Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jacquelyn","family":"Francis","sequence":"additional","affiliation":[{"name":"McKusick\u2010Nathans Institute of Genetic Medicine Johns Hopkins University Baltimore Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bernard","family":"Cohen","sequence":"additional","affiliation":[{"name":"Division of Pediatric Dermatology Johns Hopkins University Baltimore Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cozumel","family":"Pruette","sequence":"additional","affiliation":[{"name":"Division of Pediatric Nephrology Johns Hopkins University Baltimore Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Annie","family":"Grossberg","sequence":"additional","affiliation":[{"name":"Division of Pediatric Dermatology Johns Hopkins University Baltimore Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joann","family":"Bodurtha","sequence":"additional","affiliation":[{"name":"McKusick\u2010Nathans Institute of Genetic Medicine Johns Hopkins University Baltimore Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2016,7,14]]},"reference":[{"key":"e_1_2_4_2_1","doi-asserted-by":"publisher","DOI":"10.1136\/archdischild-2011-301284"},{"key":"e_1_2_4_3_1","doi-asserted-by":"publisher","DOI":"10.1186\/1750-1172-9-93"},{"key":"e_1_2_4_4_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.37004"},{"key":"e_1_2_4_5_1","first-page":"SD06","article-title":"Incontinentia pigmenti: a rare genodermatosis in a male child","volume":"9","author":"Swamy DK","year":"2015","journal-title":"J Clin Diagn Res"},{"key":"e_1_2_4_6_1","doi-asserted-by":"publisher","DOI":"10.1001\/jamapediatrics.2014.74"},{"key":"e_1_2_4_7_1","unstructured":"GeneReviews.Incontinentia Pigmenti[online].http:\/\/www.ncbi.nlm.nih.gov\/books\/NBK1472\/(accessed July 8 2015)."},{"key":"e_1_2_4_8_1","doi-asserted-by":"publisher","DOI":"10.1210\/jc.2009-2673"},{"key":"e_1_2_4_9_1","doi-asserted-by":"publisher","DOI":"10.1210\/jc.86.2.888"},{"key":"e_1_2_4_10_1","doi-asserted-by":"publisher","DOI":"10.1067\/mjd.2002.125949"},{"key":"e_1_2_4_11_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2249.2004.02310.x"},{"key":"e_1_2_4_12_1","doi-asserted-by":"publisher","DOI":"10.1359\/jbmr.060608"},{"key":"e_1_2_4_13_1","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9343(84)90674-0"},{"key":"e_1_2_4_14_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jsbmb.2006.12.078"},{"key":"e_1_2_4_15_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2133.2008.08844.x"},{"key":"e_1_2_4_16_1","doi-asserted-by":"publisher","DOI":"10.1093\/ckj\/sft046"}],"container-title":["Pediatric Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fpde.12925","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/pde.12925","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,24]],"date-time":"2023-09-24T01:08:05Z","timestamp":1695517685000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/pde.12925"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,7,14]]},"references-count":15,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2016,9]]}},"alternative-id":["10.1111\/pde.12925"],"URL":"https:\/\/doi.org\/10.1111\/pde.12925","archive":["Portico"],"relation":{},"ISSN":["0736-8046","1525-1470"],"issn-type":[{"value":"0736-8046","type":"print"},{"value":"1525-1470","type":"electronic"}],"subject":[],"published":{"date-parts":[[2016,7,14]]}}}