{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,8]],"date-time":"2025-12-08T09:05:41Z","timestamp":1765184741194,"version":"3.40.5"},"reference-count":5,"publisher":"Wiley","issue":"S2","license":[{"start":{"date-parts":[[2021,9,28]],"date-time":"2021-09-28T00:00:00Z","timestamp":1632787200000},"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":[[2021,11]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>In the dermatologic medical literature, there is an underrepresentation of conditions in individuals of color. Due to the lack of representation, it may be harder for clinicians to recognize certain diagnoses in patients with darker skin phototypes leading to misdiagnosis and affecting overall patient management, outcomes, and satisfaction. Here, we present four Black or Indigenous People of Color who were initially referred for hyperpigmentation, hemihyperplasia, or caf\u00e9 au lait spots and found to have syndromic capillary malformations.<\/jats:p>","DOI":"10.1111\/pde.14787","type":"journal-article","created":{"date-parts":[[2021,9,29]],"date-time":"2021-09-29T06:44:52Z","timestamp":1632897892000},"page":"137-139","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Misdiagnosis of capillary malformations in darker skin phototypes"],"prefix":"10.1111","volume":"38","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3006-4796","authenticated-orcid":false,"given":"Bede N.","family":"Nriagu","sequence":"first","affiliation":[{"name":"Center for Applied Genomics Children\u2019s Hospital of Philadelphia Philadelphia PA USA"},{"name":"Comprehensive Vascular Anomaly Program Children\u2019s Hospital of Philadelphia Philadelphia PA USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Victoria R.","family":"Sanders","sequence":"additional","affiliation":[{"name":"Comprehensive Vascular Anomaly Program Children\u2019s Hospital of Philadelphia Philadelphia PA USA"},{"name":"Division of Human Genetics Children\u2019s Hospital of Philadelphia Philadelphia PA USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5158-5705","authenticated-orcid":false,"given":"Lionel","family":"Bercovitch","sequence":"additional","affiliation":[{"name":"Department of Dermatology Hasbro Children\u2019s Hospital Warren Alpert Medical School Providence RI USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3209-0162","authenticated-orcid":false,"given":"Kristen","family":"Snyder","sequence":"additional","affiliation":[{"name":"Comprehensive Vascular Anomaly Program Children\u2019s Hospital of Philadelphia Philadelphia PA 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