{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T16:53:02Z","timestamp":1790873582256,"version":"4.1.0"},"reference-count":12,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2019,9,9]],"date-time":"2019-09-09T00:00:00Z","timestamp":1567987200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Pediatric Dermatology"],"published-print":{"date-parts":[[2019,11]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Although lentigines are usually benign, they can be associated with a number of genetic syndromes in which neoplasms and other multi\u2010system pathological processes occur. Here, we report the case of a 6\u2010year\u2010old girl who presented with atypical lentiginosis and hyperpigmentation caused by a de novo genetic variant in the <jats:italic>KIT<\/jats:italic> gene.<\/jats:p>","DOI":"10.1111\/pde.13952","type":"journal-article","created":{"date-parts":[[2019,9,9]],"date-time":"2019-09-09T12:20:51Z","timestamp":1568031651000},"page":"922-925","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["Novel KIT mutation presenting as marked lentiginosis"],"prefix":"10.1111","volume":"36","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-9034-918X","authenticated-orcid":false,"given":"Alain K.","family":"Tran","sequence":"first","affiliation":[{"name":"Flinders Medical Centre Adelaide South Australia Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Annette","family":"Pearce","sequence":"additional","affiliation":[{"name":"Adelaide Dermatology Associates Western Hospital Henley Beach South Australia Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marcos","family":"L\u00f3pez\u2010S\u00e1nchez","sequence":"additional","affiliation":[{"name":"Hospital del Mar Research Institute (IMIM) Network Centre for Biomedical Research in Rare Diseases (CIBERER) and Universitat Pompeu Fabra Barcelona Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Luis A.","family":"P\u00e9rez\u2010Jurado","sequence":"additional","affiliation":[{"name":"Hospital del Mar Research Institute (IMIM) Network Centre for Biomedical Research in Rare Diseases (CIBERER) and Universitat Pompeu Fabra Barcelona Spain"},{"name":"South Australian Health and Medical Research Institute University of Adelaide Adelaide South Australia Australia"},{"name":"Paediatric and Reproductive Genetic Unit Women's and Children's Hospital North Adelaide South Australia Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christopher","family":"Barnett","sequence":"additional","affiliation":[{"name":"Paediatric and Reproductive Genetic Unit Women's and Children's Hospital North Adelaide South Australia Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2019,9,9]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2796.1998.00341.x"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1007\/s10689-011-9446-x"},{"key":"e_1_2_6_4_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.2003.017806"},{"key":"e_1_2_6_5_1","doi-asserted-by":"publisher","DOI":"10.1002\/humu.23258"},{"key":"e_1_2_6_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/S1085-5629(05)80003-3"},{"key":"e_1_2_6_7_1","doi-asserted-by":"publisher","DOI":"10.1007\/s13244-012-0208-6"},{"key":"e_1_2_6_8_1","first-page":"1","article-title":"Familial Progressive Hyperpigmentation: A case report","volume":"2012","author":"Yadav M","year":"2012","journal-title":"Case Rep Dent"},{"key":"e_1_2_6_9_1","doi-asserted-by":"publisher","DOI":"10.1111\/pde.13040"},{"key":"e_1_2_6_10_1","unstructured":"Genetics Home reference 2018 U.S. National Library of Medicine KIT proto\u2010oncogene receptor tyrosine kinase.https:\/\/ghr.nlm.nih.gov\/gene\/KIT. 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