{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,16]],"date-time":"2026-02-16T18:33:41Z","timestamp":1771266821332,"version":"3.50.1"},"reference-count":23,"publisher":"Oxford University Press (OUP)","issue":"548","license":[{"start":{"date-parts":[[1971,6,1]],"date-time":"1971-06-01T00:00:00Z","timestamp":44582400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1971,6,1]]},"abstract":"<jats:title>Summary<\/jats:title>\n               <jats:p>Nine members in three generations of a Chinese family were found to have Waardenburg\u2019s syndrome comprising, mainly, lateral displacement of the inner canthi, broadening of the nasal root and hypertrichosis of the eyebrows. Other minor features were also found.<\/jats:p>\n               <jats:p>Two patients had in addition, hypokalemic periodic paralysis of the familial type, one had prominent frontal bossing and another, bilateral cleft lips and palate. These associated anomalies have not been previously documented and the presence of two autosomal dominant genetic defects in this family is of particular interest.<\/jats:p>","DOI":"10.1136\/pgmj.47.548.354","type":"journal-article","created":{"date-parts":[[2008,12,29]],"date-time":"2008-12-29T20:27:15Z","timestamp":1230582435000},"page":"354-360","source":"Crossref","is-referenced-by-count":3,"title":["Waardenburg\u2019s syndrome and familial periodic paralysis"],"prefix":"10.1093","volume":"47","author":[{"given":"C H","family":"Tay","sequence":"first","affiliation":[{"name":"Senior Medical Registrar and Clinical Teacher, Medical Unit II, Department of Clinical Medicine, University of Singapore, Outram Road General Hospital , Singapore, 3"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[1971,6,1]]},"reference":[{"key":"ref_1","first-page":"41","article-title":"The syndrome of Waardenburg","volume":"9","author":"ARNVIG, J.","year":"1959","unstructured":"ARNVIG, J. (1959) The syndrome of Waardenburg. Acta genetica et statistica medica, 9, 41.","journal-title":"Acta genetica et statistica medica"},{"key":"ref_2","article-title":"Erbleiden des Nerren systems beim","author":"BOETERS, H.","year":"1939","unstructured":"BOETERS, H. (1939) Erbleiden des Nerren systems beim"},{"key":"ref_3","first-page":"59","article-title":"In: Handbuck der Erbbiologie des Menschen","volume":"86","author":"Menschen","year":"1962","unstructured":"Menschen. In: Handbuck der Erbbiologie des Menschen (Ed. by E. Just), p. 59. Springer Verlag, Berlin. CAMPBELL, B., CAMPBELL, N.R. & SWIFT, S. (1962) Waardenburg's syndrome-a variation of the first arch syndrome. 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