{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T20:25:16Z","timestamp":1787775916436,"version":"build-2784847793"},"reference-count":11,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2018,1]]},"abstract":"<jats:p>Neu\u2013Laxova syndrome (NLS) is an autosomal recessive disorder characterized by central nervous system anomalies, facial dysmorphic features, anomalies of limb and genitalia, intrauterine growth retardation, skin disorders, and other congenital abnormalities. In this article, we present a newborn infant who was born with facial dysmorphic features, flat nose, ichthyosis, rocker bottom feet, and fixed flexion contractures. We believe that these clinical findings in this patient are consistent with features of NLS.<\/jats:p>","DOI":"10.4103\/abr.abr_143_17","type":"journal-article","created":{"date-parts":[[2018,4,23]],"date-time":"2018-04-23T06:16:48Z","timestamp":1524464208000},"update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":5,"title":["A New Case of Neu\u2013Laxova Syndrome: Infant with Facial Dysmorphism, Arthrogryposis, Ichthyosis, and Microcephalia"],"prefix":"10.4103","volume":"7","author":[{"given":"Behzad","family":"Barekatain","sequence":"first","affiliation":[{"name":"From the Department of Neonatology, Isfahan University of Medical Sciences, Isfahan, Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alireza","family":"Sadeghnia","sequence":"additional","affiliation":[{"name":"From the Department of Neonatology, Isfahan University of Medical Sciences, Isfahan, 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