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Human Monozygotic and Plurizygotic Multiple Births: Heredity and Hormone Action

Published online by Cambridge University Press:  01 August 2014

L. Gedda
Affiliation:
«Gregor Mendel» Institute for Medical Genetics, and Twin Research, Rome, (Italia)
G. Brenci
Affiliation:
«Gregor Mendel» Institute for Medical Genetics, and Twin Research, Rome, (Italia)

Summary

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The Authors take once more into consideration the problem of the hereditary nature of twinning on the basis of their own studies and of recent findings on human twinning induced by human menopausal gonadotropin (HMG).

Personal studies concern 3,221 cases of twinning drawn from the special files (“Gemelloteca”) of the Mendel Institute. On the basis of this material the Authors state that the occurrence of the cases of twinning in the paternal and maternal ascendancies of the twin index cases is significantly more frequent than would be expected in proportion to the frequency of twinning events in the Italian population.

This finding is in agreement with the hypothesis of the hereditary nature of the twinning phenomenon.

The same material is used to compare the frequency of twinning in the paternal and maternal families of twins. The observed frequency in the maternal families is significantly higher than in paternal families in which the frequency approximates population values. This finding leads the Authors to formulate the hypothesis that the twinning trait is limited to the female sex and is presently manifested by the occurrence of twins in the next generation. Thus studies on the frequency of twinning as a hereditary phenomenon should be based on the families of the mothers of twins.

Original studies also concern the 1,105 triplet sets born in Italy in the years 1952-1961. A study of the experimental and theoretical distribution of sex combinations in this triplet material allowed the Authors to prove that the experimental distribution differs from the theoretical one, based on the hypothesis of independence of the two types of zygosity (MZ and DZ). The absence of independence is considered a proof of the hereditary singleness of twinning.

The Authors further take into consideration cases of twinning induced in sterile women by administration of human menopausal gonadotropin (HMG): they observe that cases reported to date seem to be limited to dizygotic or plurizygotic twinning. These findings lead the Authors to believe that in this case hypophyseal FSH, responsible for ovulation, fails to find the usual pathway leading to standard uniparous pregnancy in the human species; the mechanism involved in such pathway is the object of some hypotheses of a hormonal nature. The Authors also believe that FSH stimulates not only the follicle but also follicular gametogenesis and even perhaps the division of the fertilized egg resulting in MZ twinning.

Type
Research Article
Copyright
Copyright © The International Society for Twin Studies 1965

References

Literature

Bonnevie, K.: Om tvillingfödslers Arvelighet. Norsk. Mag. f. Laegevidensk. 80, 8, 847868, 1919.Google Scholar
Brattström, E.: Ein Fall von viereiigen Vierlingen nebst einigen Beobachtungen betreffs der Vierlingsgeburten im allgemeinen. Monatschr. f. Geburtsh. u. Gynäk. 40, 53, 1914.Google Scholar
Bumm, : Grundriss zum Studium Geburtshilfe. Wiesbaden, 1914.Google Scholar
Cory, R.: The influence of inheritance on the tendency to have twins. Lancet, 1105, 1895.Google Scholar
Curgenven, : Hereditary twin bearing family. Tr. Obst. Soc. London, 11, 106, 1869.Google Scholar
Curtius, F., Verschuer, O. v.: Die Anlage zur Entstehung von Zwillingen und ihre Vererbung. Arch. Rass.-u. Ges.-Biol., 26, 361387, 1932.Google Scholar
Dahlberg, G.: Twin births and twins from a hereditary point of view. Inaug. Diss., Uppsala, 1926.Google Scholar
Dahlberg, G.: Eine Theorie über den Uniovulationsmechanismus mit spezieller Berücksichtigung des Follikulins. Klin. Wchnschr., 1930.Google Scholar
Danforth, C. H.: Is twinning hereditary? J. Hered., 7, 5, 195202, 1916.Google Scholar
Davenport, Ch. B.: A strain producing multiple births. J. Hered., 10, 8, 382384, 1919.Google Scholar
Davenport, Ch. B.: Heredity of twin births. Proc. Soc. Exper. Biol. & Med., N. Y., 17, 7577, 19191920.Google Scholar
Davenport, Ch. B.: Influence of the male in the production of human twins. Am. Natural., 54, 122129, 1920.Google Scholar
Davenport, Ch. B.: Influence of male on production of twins. M. Rec., 97, 17, 509, 1920.Google Scholar
Debiasi, E.: Le gonadotropine nella terapia della infertilità maschile da oligoastenospermia. Proc. of the Intern. Symp. « Male and Female Sterility. Treatment with Human Gonadotropins ». Rome, 1965.Google Scholar
Donini, P.: Le gonadotropine umane. Purificazione e separazione dell'ormone follicolo-stimolante urinario (FSH) dall'ormone luteinizzante (ICSH). Proc. of the Intern. Symp. «Male and Female Sterility. Treatment with Human Gonadotropins», Rome, 1965.Google Scholar
Eckert, E.: Die Zwillingsgeburten im Oberamt Tübingen aus den Jahren 1901-1925. Diss. Tübingen, 1928.Google Scholar
Feré, : Folies gémellaires. Compt. rend. Soc. Biol., Paris, 1902.Google Scholar
Fisher, R. A.: The genesis of twins. Genetics, 4, 89499, 1919.Google Scholar
Fisher, R. A.: The genesis of twins. Lancet, 1, 736, 1920.Google Scholar
Fisher, R. A.: New data on the genesis of twins. Eugenics Review, 14, 115117, 19221923.Google Scholar
Gedda, L.: Investigation of twins in Italy. Proc. of the 8th Intern. Cong, of Genet., Stockholm, 1949.Google Scholar
Gedda, L.: Lo studio dei gemelli nella scienza. Minerva Medica, XLI–II, 37, 1950.Google Scholar
Gedda, L.: Studio dei gemelli. Ediz. Orizzonte Medico, Roma, 1951.Google Scholar
Gedda, L.: Twin studies. Eugenics Quarterly, I, 3, 1954.Google Scholar
Gedda, L.: Twins in history and science. Charles C Thomas, Springfield, 1961.Google Scholar
Gedda, L.: La sterilità disendocrina ipofisaria. Il suo profilo genetico ed il suo significato biologico. Proc. of the Intern. Symp. « Male and Female Sterility. Treatment with Human Gonadotropins », Rome, 1965.Google Scholar
Gedda, L.: Brenci, G.: Lo studio dei gemelli come metodo di ricerca in genetica umana, in De Genetica Medica, Pars II, Ediz. Istituto Mendel, Roma, 1962.Google Scholar
Gemzell, C. A.: Therapy of gynecological disorders with human gonadotropin. Vitamins and Hormones, 22, 129151, 1964.CrossRefGoogle ScholarPubMed
Gemzell, C. A.: Induction of ovulation in the human by human gonadotrophins. Progress in Gynecology. IV, 187198, 1963.Google Scholar
Gemzell, C. A.: and Kjessler, Berndt: Treatment of infertility after partial hypophysectomy with human pituitary gonadotrophins. The Lancet, 03 21, 644, 1964.Google Scholar
Greulich, W. W.: Heredity in human twinning. Amer. J. physic. Anthrop., 19, 391431, 1934.CrossRefGoogle Scholar
Grigg, W. C.: Heredity as to triplets. Brit. M. J., 1, 541, 1890.Google Scholar
Heller, C. G. and Clermont, Yves: Kinetics of the germinal epithelium in man. Rec. Prog. Horm. Res. 20 545575 (1964).Google Scholar
Hofsten, N. V.: Arftlighetslära. Uppsala, 1919.Google Scholar
Jenkins, R. L.: Twin and triplet birth ratios; inter-relations of frequencies of plural births. J. Hered., 18, 1927.Google Scholar
Jullien, L. J. E. G.: Documents statistiques concernant l'étude des grossesses gémellaires. Diss., Paris, 1897.Google Scholar
Lauritzen, W.: Om Svangerskab og Fodsel ved Tvillinger. Diss. Kobenhavn, 1891.Google Scholar
Lenz, F.: Zur genetischen Deutung von Zvillingsbefunden. Ztschr. indukt. Abstam. u. Vererbgslehre, 52, 1933.Google Scholar
Lunenfeld, B.: Treatment of anovulation by human gonadotrophins. Journal of the International Federation of Gynecology and Obstetrics. I. 3-07 1963.Google Scholar
Lunenfeld, B.: L'influence des gonadotropines humaines sur le développement testiculaire. Proc. of the Intern. Symp. « Male and Female Sterility. Treatment with Human Gonadotropins ». Rome, 1965.Google Scholar
Lunenfeld, B.: Eshkol, A., Donini, P., Puzzuoli, D. and Shelesnyak, M. C.: Studies on gonadotropins: C. Biological assessment of highly purified urinary extracts. Harokeach Haivri (The Hebrew Pharmacist), Scientific edition 9: 766 (1963).Google Scholar
Lunenfeld, B.: Donini, P.: Le traitement de l'anovulation par les hormones gonadotropes humaines. L'insuffisance lutéale, VIIe Réunion des Endocrinologistes de langue française. Massou Ed. Paris 335354 (1963).Google Scholar
MacLeod, J.: The restoration of human spermatogenesis (following hypophysectomy) with menopausal gonadotropins. Proc. of the Intern. Symp. « Male and Female Sterility. Treatment with Human Gonadotropins », Rome, 1965.Google Scholar
Masson, A.: De l'hérédité des grossesses gémellaires. Gaz. obst. et gynéc. de Paris, 1876.Google Scholar
Melmann, F.: Influence de la lignée masculine dans la production des grossesses gémellaires. Genève, 1910.Google Scholar
Meyer, R.: Questione della superfetazione. Ztschr. f. Geburtsh. u. Gynäk., 5, 214, 1923 (Deutsch).Google Scholar
Mirabeau, S.: Inaug. Diss., München, 1894.Google Scholar
Neuwirth, R. S., Todd, W. D., Turksoy, R. N. and Vande Wiele, R. L.: Successful quadruplet pregnancy in a patient treated with human menopausal gonadotropins. American Journal of Obstetrics and Gynecology, 91, 7, 982–904, 04 1, 1965.Google Scholar
Pasetto, N.: Le gonadotropine umane nella terapia della sterilità maschile. Proc. of the Intern. Symp. « Male and Female Sterility, Treatment with Human Gonadotropins », Rome, 1965.Google Scholar
Peiper, A.: Zur Vererbung der Zwillingsschwangerschaft durch der Mann. Klin. Wochnschr., 2, 25, 1923.Google Scholar
Rabau, E.: New aspects in the treatment of Ghiari-Frommel and Sheehan syndromes. Proc. of the Intern. Symposium « Male and Female Sterility. Treatment with Human Gonadotropins », Rome, 1965.Google Scholar
Siemens, H. W.: Einführung in die allgemeine und spezielle Vererbungspathologie des Menschen. Berlin, 1923.Google Scholar
Siemens, H. W.: Diagnosis of identity in twins. J. Hered., 18, 5, 201209, 1927.Google Scholar
Speyer, Th. v.: Die mehrfachen Geburten in ihren erblichen Beziehungen. Inaug. Diss., Basel, 1894.Google Scholar
Stoker, M.: A case of quintuplets. Brit, gynec. J., 11, 373, 1896.Google Scholar
Vande Wiele, R. L., Turksoy, R. N.: Treatment of amenorrhea and of anovulation with human menopausal and chorionic gonadotropins. The Journal of Clinical Endocrinology and Metabolism, 25, 3, 03, 369384, 1965.Google Scholar
Vande Wiele, R.: Stimulation of ovarian function in post-hypophysectomy cases. Proc. of the Intern. Symp. « Male and Female Sterility. Treatment with Human Gonadotropins», Rome 1965.Google Scholar
Verschuer, O. v.: Buchbesprechung Dahlberg G.: “ Twin births and twins from a hereditary point of view. ” 1926. Arch. Rass.-u. Ges.-Biol., 19, 1, 8892, 1927.Google Scholar
Wakley, : The influence of inheritance on the tendency to have twins. Lancet, 2, 1289, 1895.Google Scholar
Wehefritz, E.: Ueber die Vererbung der Zwillingsschwangerschaft. Ztschr. f. Konstitutionslehre, 11, II–V, 554575, 1925.Google Scholar
Weinberg, W.: Die Anlage zur Mehrlingsgeburt beim Menschen und ihre Vererbung. Arch. Rass.-u. Ges.-Biol., 6, 3, 322, 1909.Google Scholar
Wilson, P. Th.: A study of like-sexed twins; twinning among relatives. J. Hered., 21, 8, 371, 1930.CrossRefGoogle Scholar
Yerushalmy, J., Sheerar, S. E.: Studies on twins. I. The relation of order of birth and age of parents to the frequency of like-sexed and unlike-sexed twin deliveries. Human Biol., 12, 95113, 1940.Google Scholar
Yerushalmy, J., Sheerar, S. E., Studies on twins. II. On the early mortality of like-sexed and unlike-sexed twins. Human Biol., 12, 247263, 1940.Google Scholar