{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,5]],"date-time":"2026-05-05T22:35:24Z","timestamp":1778020524624,"version":"3.51.4"},"reference-count":17,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2022,5,23]],"date-time":"2022-05-23T00:00:00Z","timestamp":1653264000000},"content-version":"vor","delay-in-days":22,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clinical Case Reports"],"published-print":{"date-parts":[[2022,5]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Feingold syndrome 1 (FS1) is a rare disorder that is inherited in autosomal dominant manner with full penetrance but with variable expressivity. The most common phenotypical features described are finger and toe anomalies, microcephaly, short stature, and intestinal atresia. Dysmorphic features, intellectual disability and other organ anomalies are less frequently described. Here, we present a 7\u2010year\u2010old boy with severe intellectual disability who is diagnosed with FS1\u00a0syndrome caused by a new heterozygous variant of MYCN gene<\/jats:p>","DOI":"10.1002\/ccr3.5886","type":"journal-article","created":{"date-parts":[[2022,5,23]],"date-time":"2022-05-23T04:55:45Z","timestamp":1653281745000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["A new variant of MYCN gene as a cause of Feingold syndrome"],"prefix":"10.1002","volume":"10","author":[{"given":"Naim","family":"Zeka","sequence":"first","affiliation":[{"name":"Pediatric Clinic Department of Neurology University Clinical Center of Kosovo  Pristina Kosovo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ramush","family":"Bejiqi","sequence":"additional","affiliation":[{"name":"Pediatric Clinic Department of Cardiology University Clinical Center of Kosovo  Pristina Kosovo"},{"name":"Faculty of Medicine University of Gjakova  Pristina Kosovo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Abdurrahim","family":"Gerguri","sequence":"additional","affiliation":[{"name":"Pediatric Clinic Department of Neurology University Clinical Center of Kosovo  Pristina Kosovo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Leonore","family":"Zogaj","sequence":"additional","affiliation":[{"name":"Pediatric Clinic Department of Neurology University Clinical Center of Kosovo  Pristina Kosovo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4577-8604","authenticated-orcid":false,"given":"Haki","family":"Jashari","sequence":"additional","affiliation":[{"name":"Pediatric Clinic Department of Neurology University Clinical Center of Kosovo  Pristina Kosovo"},{"name":"Pediatric Clinic University Children\u2019s Hospital  Skopje Republic of North 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