{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,6,10]],"date-time":"2025-06-10T05:44:23Z","timestamp":1749534263331},"reference-count":8,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2013,11,21]],"date-time":"2013-11-21T00:00:00Z","timestamp":1384992000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Forensic Sciences"],"published-print":{"date-parts":[[2014,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>In the course of applying to become a soldier, a 23\u2010year\u2010old <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>audi <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>rabian man was found to have no fingerprints. Further medical examination has been carried out for the young man and for the rest of family members including two sisters, mother, and brothers except the father who had died sometime previously. Subsequent medical investigations suggested that he and his two brothers displayed most of the features of the <jats:styled-content style=\"fixed-case\">N<\/jats:styled-content>aegeli\u2013<jats:styled-content style=\"fixed-case\">F<\/jats:styled-content>ranceschetti\u2013<jats:styled-content style=\"fixed-case\">J<\/jats:styled-content>adassohn (<jats:styled-content style=\"fixed-case\">NFJ<\/jats:styled-content>) syndrome. These features included skin changes with hypo\u2010 and hyperpigmentation, hypohidrosis, dystrophy of the nails, diffuse thickening of the palms and feet, a lack of fingerprints (dermatoglyphics), and atrophic changes in the skin of the face; there were also dental anomalies. A typical feature of the <jats:styled-content style=\"fixed-case\">N<\/jats:styled-content>aegeli\u2013<jats:styled-content style=\"fixed-case\">F<\/jats:styled-content>ranceschetti\u2013<jats:styled-content style=\"fixed-case\">J<\/jats:styled-content>adassohn syndrome was found in a <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>audi <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>rabian family. The aim of this study was to present this rare condition affecting a <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>audi <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>rabian family and review the current literature on the subject.<\/jats:p>","DOI":"10.1111\/1556-4029.12316","type":"journal-article","created":{"date-parts":[[2013,11,21]],"date-time":"2013-11-21T21:55:39Z","timestamp":1385070939000},"page":"555-558","source":"Crossref","is-referenced-by-count":7,"title":["Naegeli\u2013Franceschetti\u2013Jadassohn Syndrome in a Saudi Arabian Family"],"prefix":"10.1111","volume":"59","author":[{"given":"Salah M.","family":"Tubaigy","sequence":"first","affiliation":[{"name":"Department of Medico Legal Medicine Public Security Ministry of Interior P.O. Box 103223 Riyadh 11695 Saudi Arabia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H. 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