{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,9]],"date-time":"2026-05-09T04:07:11Z","timestamp":1778299631337,"version":"3.51.4"},"reference-count":18,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2020,9,28]],"date-time":"2020-09-28T00:00:00Z","timestamp":1601251200000},"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":[[2021,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Hereditary sensory and autonomic neuropathy (HSAN) type IV, also known as congenital insensitivity to pain with anhidrosis (OMIM 256800), is part of a family of neurodegenerative disorders that manifest with variable sensory and autonomic neuropathies. In this report, we present a unique dermatological finding in a patient with HSAN type IV: bilateral harlequin syndrome that occurred in association with unilateral Horner syndrome, traumatic alopecia and Riga\u2010Fede disease.<\/jats:p>","DOI":"10.1111\/pde.14385","type":"journal-article","created":{"date-parts":[[2020,9,28]],"date-time":"2020-09-28T10:50:57Z","timestamp":1601290257000},"page":"213-216","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["Bilateral harlequin syndrome, unilateral Horner syndrome, and Riga\u2010Fede disease as presenting features of hereditary sensory and autonomic neuropathy type IV"],"prefix":"10.1111","volume":"38","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-2543-3526","authenticated-orcid":false,"given":"Saud","family":"Alobaida","sequence":"first","affiliation":[{"name":"Department of Dermatology and Skin Sciences University of British Columbia Vancouver BC Canada"},{"name":"Department of Dermatology King Faisal Specialist Hospital &amp; Research Centre Riyadh Saudi Arabia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7808-3369","authenticated-orcid":false,"given":"Joseph M.","family":"Lam","sequence":"additional","affiliation":[{"name":"Department of Dermatology and Skin Sciences University of British Columbia Vancouver BC Canada"},{"name":"Department of Pediatrics and Department of Dermatology and Skin Sciences University of British Columbia Vancouver BC Canada"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2020,9,28]]},"reference":[{"key":"e_1_2_4_2_1","doi-asserted-by":"publisher","DOI":"10.1097\/01.wco.0000245370.82317.f6"},{"key":"e_1_2_4_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.nbd.2005.08.004"},{"key":"e_1_2_4_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.pediatrneurol.2016.04.006"},{"key":"e_1_2_4_5_1","doi-asserted-by":"publisher","DOI":"10.1542\/peds.112.3.e237"},{"key":"e_1_2_4_6_1","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/awp198"},{"key":"e_1_2_4_7_1","doi-asserted-by":"publisher","DOI":"10.1111\/ped.12538"},{"key":"e_1_2_4_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.mayocp.2013.02.018"},{"key":"e_1_2_4_9_1","first-page":"1993","volume-title":"GeneReviews\u00ae","author":"Indo Y"},{"key":"e_1_2_4_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jaad.2016.12.031"},{"key":"e_1_2_4_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.bjps.2007.04.008"},{"issue":"3","key":"e_1_2_4_12_1","first-page":"173","article-title":"The, \"harlequin sign\". 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