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We present a case of a 4\u2010year\u2010old boy diagnosed with NSLD, presenting with multiple melanocytic nevi and superficial neurofibromas. A literature review identified common cutaneous findings of NSLD, for example, caf\u00e9\u2010au\u2010lait macules (22%), juvenile xanthogranuloma (16%), and thin hair (10%). As there are no documented cases of neurofibromas associated with NSLD, and only a single report of multiple melanocytic nevi, inclusion of these features in the phenotype may be warranted and mitigate the necessity for future biopsies in other children.<\/jats:p>","DOI":"10.1111\/pde.15696","type":"journal-article","created":{"date-parts":[[2024,7,30]],"date-time":"2024-07-30T07:34:32Z","timestamp":1722324872000},"page":"1203-1210","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Noonan syndrome\u2010like disorder: Case report and review of the literature"],"prefix":"10.1111","volume":"41","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2482-8633","authenticated-orcid":false,"given":"Kristie","family":"Mar","sequence":"first","affiliation":[{"name":"Faculty of Medicine University of British Columbia  Vancouver British Columbia 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