Hostname: page-component-cd9895bd7-lnqnp Total loading time: 0 Render date: 2024-12-25T02:11:18.299Z Has data issue: false hasContentIssue false
  • English
  • Français

Sul diabete giovanile misto famigliare

Published online by Cambridge University Press:  01 August 2014

Domenico Casa
Domenico Casa*
Affiliation:
Istituto di Genetica Medica e Gemellologia, “G. Mendel” - Direttore: Prof. Luigi Gedda, Diabetarium Pediatrico Nazionale P. O. A.

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The A. presents the case of two sisters, both affected by mixed juvenile diabetes: diabetes mellitus and diabetes insipidus.

Three of their brothers died of diabetes millitus.

After discussing different etiological hypotheses, the A. indicates the hereditary one as the most likely.

Probably, in the case of the two sisters, there was an association of two hereditary processes, independent of one another, but coexistent.

Riassunto

RIASSUNTO

L'A. presenta due sorelle entrambe malate di diabete misto giovanile: diabete mellito e diabete insipido. Esse appartengono ad una fratria dove altri tre fratelli sono morti per diabete mellito. Dopo aver discusso diverse ipotesi etiologiche, quella ereditaria sembra essere la più soddisfacente. Probabilmente nelle sorelle studiate si è verificata un'associazione di due processi ereditari indipendenti ma coesistenti.

Résumé

RÉSUMÉ

L'A. présente deux sœurs, toutes les deux atteintes de diabète mixte juvénile: diabète sucré et diabète insipide.

Elles appartiennent à un groupe de frères et de sœurs, dont déjà trois frères sont morts de diabète sucré.

Après avoir discuté les différentes hypothèses étiologiques, celle de l'hérédité semble la plus vraie.

Probablement, dans le cas des deux sœurs, s'est vérifiée une association de deux processus héréditaires indépendants mais co-existants.

Zusammenfassung

ZUSAMMENFASSUNG

Der Verfasser stellt uns zwei Schwestern vor, die an gemischter Jugendzuckerkrankheit leiden (Diabetes mellitus und insipidus). Beide gehören einer Sippe an, aus der schon drei Brüder an Diabetes mellitus gestorben sind. Nachdem der Verfasser die verschiedensten Gründe, die Ursache der Krankheit sein könnten studiert hat, entscheidet er sich für die Vererbungsanlage. Wahrscheinlich sind bei den Schwestern zwei Erbströme, die zwar unabhängig aber dach gleichzeitig bestanden, zusammengetroffen.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 4 , Issue 2 , May 1958 , pp. 230 - 241
Copyright
Copyright © The International Society for Twin Studies 1956

References

Bibliografía

Allen, F. M., Mitchell, J. W.: Arc. Int. Med. 25, 648, 1920.Google Scholar
Andreu, Urra J.: Hipófisis y diabetes. Sevilla 1952.Google Scholar
Barach, J. H.: Am. J. M. Sc. 172, 243, 1926.CrossRefGoogle Scholar
Barker, O. B., Commons, R. R., Shelton, E. K.: J. Clin. Endoc. 11, 608, 1951.CrossRefGoogle Scholar
Camelin, A., Garnung, H., Loup, R.: B. et M. des hopitaux de Paris. 1951 67° Ann., 23–24.Google Scholar
Cammidge, P. J., Howard, H. A. H.: J. Genetics. 16, 387, 1926.CrossRefGoogle Scholar
Cole, V., Harned, B. K., Keeler, C. E.: End. 28, 25, 1941.Google Scholar
Conde, Gargollo E.: Rev. Clin. Espan. 3, 61, 1955.Google Scholar
Deshmukh, P. L. J.: Ind. Med. Ass. 23, 3, 1953.Google Scholar
Dolle, W. Z. Menschl. Vereb. U. Konstit. Lehere. 30, 3, 372, 1951.Google Scholar
Faelli, C.: Diabetologia Clinica. 1942.Google Scholar
Faelli, C.: Il Diabete nella Medicina Sociale. 1954.Google Scholar
Faelli, C.: Acta Med. Scand. Suppl. 159, 1945.Google Scholar
Forssman, H. A. J. of Human Genetics 1, 7, 1955.Google Scholar
Forssman, H. A. Acta Med. Scand. Suppl. 159, 1945.Google Scholar
Gedda, : Studio dei gemelli. Orizzonte Medico, 1951.Google Scholar
Haldane, J. B. S. J.: Genetics. 41, 149, 1941.Google Scholar
Hanhart, E.: Helvet. Med. Acta. 14, 243, 1947.Google Scholar
Harris, H.: Ann. Eugenics. 14, 293, 1949.Google Scholar
Harris, H.: Proc. Roy. Soc. Med. 42, 326, 1949.Google Scholar
Harris, H.: Ann. Eugenics. 15, 95, 1950.Google Scholar
Harris, H.: Ann. Eugenics. 15, 95, 1950.Google Scholar
Harris, H., Kalmus, H., Trotter, W. R.: Lancet. 257, 1038, 1949.CrossRefGoogle Scholar
Joslin, E. P.: Journ. Am. Med. Ass. 85, 420. 1925.CrossRefGoogle Scholar
Lafuente, A.: Boll. Inst. Patol. Med. 6, 121, 1951.Google Scholar
Landis, H. R. M.: Tr. A. Am. Physicians. 36, 293, 1921.Google Scholar
Levit, S. G., Pessikova, L. N.: Proc. Max. Gorky Med. Biol. Inst. Mosca. 3, 132, 1934.Google Scholar
Lowrei, G. H., Arbor, A.: Am. J. Of Dis. in Child., 80, 1, 1950.Google Scholar
Mamou, H.: Sem. Hop. Paris. 29, 26, 1306, 1953.Google Scholar
Maranon, G.: El crecimiento y sus trastornos. 1953.Google Scholar
Marinosci, A.: Folia endocrinologica. 6, 7, 1954.Google Scholar
Mayer, J.: Science, 113, 746, 1951. End., 50, 318, 1952.Google Scholar
Munro, H. N., Raton, J. C., Glen, A. J.: Clin. End., 9, 48, 1949.CrossRefGoogle Scholar
Penrose, L. S.: Ann. Eugenics. 6, 133, 1935.Google Scholar
Penrose, L. S.: Ann. Eugenics. 13, 25, 1946.Google Scholar
Penrose, L. S.: Ann. Eugenics. 15, 243, 1950.Google Scholar
Penrose Watson, E. M.: Proc. Am. Diabetes. A. 5, 163, 1945.Google Scholar
White, Pincus: Am. J. M. Sc. 186, 1, 1933.CrossRefGoogle Scholar
Keeler, Rudy: New England J. Med. 221, 329, 1939.Google Scholar
Segall, G.: J. Hered. 39, 228, 1948.Google Scholar
Arnold, Sorsby: Clinical Genetics. 1953.Google Scholar
Terry, M. C., Segall, G.: J. Hered. 38, 135, 1947.Google Scholar
Thompson, M. W., Laakso, L. E., Watson, E. M.: Can. M. A. J. 63, 556, 1950.Google Scholar
Waring, J. A., Kajdi, L., Tappan, A.: Res. Nerv. Ment. Dis. Child. Proc. (1936) 17, 392, 1938.Google Scholar
Watson, E. M., Thompson, M. W.: Am. J. Digest. Dis. 18, 326, 1951.Google Scholar
Williams, R. H., Henry, C.: Ann. Int. Med. 27, 84, 1947.Google Scholar
Wylie Mary, E. S.: Arc. of Dis. in Child. 28, 140, 1953.Google Scholar