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Considerazioni Sulla Sordità Congenita Ereditaria Apparentemente Legata Al Sesso

Published online by Cambridge University Press:  02 February 2016

G. De Vido  and
G. B. De’ Stefani
G. De Vido
Affiliation:
Clinica Otorinolaringoiatrica della Università di Padova
G. B. De’ Stefani
Affiliation:
Clinica Otorinolaringoiatrica della Università di Padova

Summary

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After some brief considerations about the etiopatogenesis of the hereditary deafness, and the modern classification of its different nosologic pictures, the AA. pass on to consider four cases of female sex, two sisters and two cousins of mother side, with hereditary familiary deafness, apparently boun to the sex. All the four cases are characterized by the identity of the audiometrie findings, after the « Law of the symmetry of the hereditary deafness ».

The AA. discuss at least the modality of the hereditary transmission and the anatomopatologic picture of the morbide form.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 1 , Issue 3 , September 1952 , pp. 294 - 306
Copyright
Copyright © The International Society for Twin Studies 1952

References

Bibliografia

Albrecht, W., Arch, fur Ohren. Bd. 110 15, 53, 1923.Google Scholar
Azzi, A., Corso di audilogia. Milano, 1951.Google Scholar
Benjamin, H., Acta Otolaryng. XXVII, 508, 1939.Google Scholar
Bunch, C. C., Clinical Budiometry. St. Louis, 1943.Google Scholar
Calvet, J., De Auditione Restituendo,. Lausanne, 1950.Google Scholar
Carrea Netto, RevistaBrasileira de Oto. 14, 5, 1946 (Exc. Medica).Google Scholar
Eggston, A. A. and Wolff, D., Hystopathology of Ear. Baltimore, 1947.Google Scholar
Eicken, V., Acta Oto-Laryng. XXVII, 503, 1950.Google Scholar
Ersner, M. S. and Saltzmann, M., Laryngoscope, LI, 3, 241, 1941.Google Scholar
Fowler, E. P., Medicine of the Ear. Nelson, New York, 1948.Google Scholar
Gedda, L., Studio dei gemelli. Orizz. Med. Koma, 1951.Google Scholar
Gedda, L., Acta geneticae medicae et gemellologiae, 1, 7, gen. 1952.Google Scholar
Gedda, L., Medica, Minerva, vol. II, n. 63, pag. 397, settembre 1951.Google Scholar
Gedda, L., Medica, Minerva, vol. I, n. 19, 5 marzo 1952.Google Scholar
Goldstein, M. A., Arch. Otolaryng., 24, 676, 1936.Google Scholar
Goodhill, S., Annals Otol. Rhin. & Laryng., 59, 4, 1950.Google Scholar
Gradenigo, G., La surdité familiale, Paris, 1921.Google Scholar
Guggenhein, L. K., Arch. Otolaryng., 803, 1936.Google Scholar
Jackson, CH. and Jackson, CH. L., Disease of the Nose, Throat and Ear. W. B. Saunders Company, Philadelphia and London, 1946.Google Scholar
Kinney, E., Annals Otol. Rhin. & Laryng. 59, 4, 1950.Google Scholar
Kobrak, A., Acta oto-laryng. 35, 6, 66, 1948.Google Scholar
Kristensen, H. K., Acta oto-laryngol. 36, 1, 60, 1948.Google Scholar
Lange, W., Zeitschrift für Ohren. 1, 14, 1937.Google Scholar
Langenbeck, B., Zeitschrift für Ohren. 223, 261, 1936.Google Scholar
Nusdorfer, R., Il Valsalva, 2, 44, 1943.Google Scholar
Ojala, L., Acta Otolaryng., 127, 1943.Google Scholar
Saltzmann, M., Clinical Audiology. New York, 1949.Google Scholar
Luchsinger, R.und Hanhart, E., (citato da Gedda). Arch. f. Klaus-Stiftg. 24, 417, 1949.Google Scholar
Shambaugh, E. JR. and Shambaugh, G. E., Arch. Otolaryng., 17, 171, 1933 (citato da Gedda).Google Scholar
Reich, Vogelsang und Barth, , Erbl. Hals usw. Arzt. 34, 1937 (citato da Gedda).Google Scholar
Ulrich, S., Acta Otolaryng. XXVII, 505, 1939.Google Scholar