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Title: [Radioulnar synostosis as characteristic feature of chromosome aberrations (author's transl)]. Author: Küsswetter W, Heisel A. Journal: Z Orthop Ihre Grenzgeb; 1981 Feb; 119(1):10-3. PubMed ID: 7281903. Abstract: Among 13 patients with congenital proximal radioulnar synostosis the chromosomal analysis revealed a 47, XXY-constellation in an 8 years old boy and a 47, XXX-syndrome in a 12-year-old girl. The investigations show, that the congenital radio-ulnar synostosis may be combined with the chromosome aberration more often than it was commonly thought.[Abstract] [Full Text] [Related] [New Search]