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This association is probably inherited as an incomplete dominant trait, apparently as a result of a new mutation.<\/jats:p><jats:p>In this case a single pleiotropic gene might be held responsible for the multiple skeletal defects.<\/jats:p><jats:p>From a bibliographical review, it may be concluded that the nosological association of these multiple defects has never been published so far.<\/jats:p>","DOI":"10.1017\/s1120962300014578","type":"journal-article","created":{"date-parts":[[2016,7,27]],"date-time":"2016-07-27T09:51:25Z","timestamp":1469613085000},"page":"534-545","source":"Crossref","is-referenced-by-count":7,"title":["Congenital Coxa Vara, Patella Aplasia and Tarsal Synostosis: <i>A New Inherited Syndrome<\/i>"],"prefix":"10.1017","volume":"19","author":[{"given":"L.","family":"Goeminne","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Dujardin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"56","published-online":{"date-parts":[[2014,8,1]]},"reference":[{"key":"S1120962300014578_ref016","first-page":"41","article-title":"Familial synostosis of autopodium and a discussion of its causes","volume":"23","author":"Slaby","year":"1964","journal-title":"Plzen. lek. 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