{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,13]],"date-time":"2026-03-13T20:55:54Z","timestamp":1773435354540,"version":"3.50.1"},"reference-count":25,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2017,12,7]],"date-time":"2017-12-07T00:00:00Z","timestamp":1512604800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clinical Case Reports"],"published-print":{"date-parts":[[2018,1]]},"abstract":"<jats:title>Key Clinical Message<\/jats:title>\n                  <jats:p>48, XYYY syndrome is a rare condition. A male with 32\u2010year\u2010old and three Y chromosomes is described. This syndrome is phenotypically similar to Klinefelter syndrome. In this patient, Semi\u2010Klinefelter characteristics such as tall stature, teeth dysmorphology, long length of fingers, partial deformity of the joints, likewise mental health problems were obvious.<\/jats:p>","DOI":"10.1002\/ccr3.1311","type":"journal-article","created":{"date-parts":[[2017,12,7]],"date-time":"2017-12-07T03:16:40Z","timestamp":1512616600000},"page":"179-184","source":"Crossref","is-referenced-by-count":3,"title":["Rare 48,\n                    <scp>XYYY<\/scp>\n                    syndrome: case report and review of the literature"],"prefix":"10.1002","volume":"6","author":[{"given":"Maryam","family":"Abedi","sequence":"first","affiliation":[{"name":"Department of Animal Science Faculty of Natural Sciences Tabriz University Tabriz Iran"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6141-3915","authenticated-orcid":false,"given":"Arash","family":"Salmaninejad","sequence":"additional","affiliation":[{"name":"Drug Applied Research Center Student Research Committee Tabriz University of Medical Sciences Tabriz Iran"},{"name":"Medical Genetics Research Center Student Research Committee Department of Medical Genetics Faculty of Medicine Mashhad University of Medical Sciences Mashhad Iran"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ebrahim","family":"Sakhinia","sequence":"additional","affiliation":[{"name":"Connective Tissue Research Center Department of Medical Genetics Faculty of Medicine and Tabriz Genetic Analysis Centre (TGAC) Tabriz University of Medical Sciences Tabriz Iran"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2017,12,7]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF01213097"},{"key":"e_1_2_7_3_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00431-014-2267-9"},{"key":"e_1_2_7_4_1","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1186\/s12881-017-0371-1","article-title":"Autism spectrum disorder associated with 49, XYYYY: case report and review of the literature","volume":"18","author":"Demily C.","year":"2017","journal-title":"BMC Med. 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