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A roentgenologic and genetic study of a rare osseous distrophy

Published online by Cambridge University Press:  01 August 2014

D. O. Ilha  and
F. M. Salzano
D. O. Ilha
Affiliation:
Departamento de Genética, Instituto de Ciências Naturais, Universidade do Rio Grande do Sul, Pôrto Alegre, Brazil
F. M. Salzano
Affiliation:
Departamento de Genética, Instituto de Ciências Naturais, Universidade do Rio Grande do Sul, Pôrto Alegre, Brazil

Summary

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Description is made of a family of which in three generations five members presented a rare osseous distrophy. Medical information was obtained for about 46 individuals of the 107 who constitute the family. The affection shows resemblances with both the Camurati-Engelmann disease and hyperostosis corticalis generalisata familiaris. It is inherited through a dominant gene.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 10 , Issue 3 , July 1961 , pp. 340 - 352
Copyright
Copyright © The International Society for Twin Studies 1961

References

Buchem, F. S. P., Hadders, H. N. and Ubbens, R. 1955: An uncommon familial systemic disease of the skeleton: Hyperostosis corticalis generalisata familiaris. Acta Radiol., 44: 109–120.Google Scholar
De Souza, O. 1927: Leontiasis ossea. Rev. dos Cursos, Faculdade de Medicina de Pòrto Alegre, Brazil, 13: 47–54.Google Scholar
Neuhauser, E. B. D., Schwachmann, H., Wittenborg, M., and Cohen, J. 1948: Progressive diaphyseal dysplasia. Radiology, 51: 11–22.Google Scholar
Ribbing, S. 1949: Hereditary multiple diaphyseal sclerosis. Acta Radiol., 31: 522–536.Google Scholar
Schinz, H. R., Baensch, W. E., Friedl, E. and Uehlinger, E. 1951: Roentgendiagnostics. English Edition, Grune Stratton. New York.Google Scholar
Uehlinger, E. 1941: Hyperostosis generalisata mit Pachydermia (idiopathische familiäre generalisierte Osteophytose Friedreich-Erb-Arnold). Virchow's Arch. path. Anat. 308: 396. Cited by Schinz et al., 1951.Google Scholar