Hostname: page-component-848d4c4894-cjp7w Total loading time: 0 Render date: 2024-06-27T05:50:29.877Z Has data issue: false hasContentIssue false
  • English
  • Français

Étude d'un Couple de Jumeaux Monozygotes dont un seul est atteint de Myopathie (Forme Pseudo-Hypertrophique)1

Published online by Cambridge University Press:  01 August 2014

J. de Grouchy ,
M. Lamy ,
J. Frézal  and
R. Garcin
J. de Grouchy
Affiliation:
Clinique de Génétique Médicale, Hôpital des Enfants-Malades, Paris (France)
M. Lamy
Affiliation:
Clinique de Génétique Médicale, Hôpital des Enfants-Malades, Paris (France)
J. Frézal
Affiliation:
Clinique de Génétique Médicale, Hôpital des Enfants-Malades, Paris (France)
R. Garcin
Affiliation:
Clinique de Génétique Médicale, Hôpital des Enfants-Malades, Paris (France)

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 Authors report on a pair of MZ twins, only one of which affected by the Duchenne-type myopathy. Monozygosity is supported by the success of a reciprocal skin-graft.

Various hypotheses are discussed, including that of a somatic mutation during the first division of the egge producing the twins.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 12 , Issue 4 , October 1963 , pp. 324 - 334
Copyright
Copyright © The International Society for Twin Studies 1963

Footnotes

1

Travail réalisé avec l'aide de l'lnstitut National d'Hygiène, et du National Institute of Health, U.S.A. (Grant N. M-3921).

References

Bibliographie

1. Dreyfus, J. C., Schapira, G., Sohapira, F. & Demos, J., 1961: Sur la détection des hétérozygotes dans la myopathie. Proceedings of the Second International Congress of Human Genetics, Rome 1961.Google Scholar
2. Jacobs, P. A., Harnden, D. G., Buckton, K. E., Court-Brown, W. M., King, H. J., McBride, J. A., MacGregor, T. N. & Maclean, N., 1961: Cytogenetic studies in primary amenorrhoea. Lancet, 1: 1183.CrossRefGoogle ScholarPubMed
3. Lamy, M. & de Grouchy, J., 1955: L'hérédité de la myopathie (formes basses). J. Genet. Hum., 3: 219.Google Scholar
4. Lejeune, J. & Turpin, R., 1961: Détection chromosomique d'une mosaïque artificielle humaine. C. R. Acad. Sc. Paris, 252: 3148.Google Scholar
5. Lindsten, J., 1951: New type of chromosomal mosaicism in ovarian dysgenesis. Lancet, 1: 1228.Google Scholar
6. Michelson, A. M., Russel, E. S. & Pincknee, J. H., 1955: Dystrophia muscularis: a hereditary primary myopathy in the house mouse. Proc. Nat. Acad. Sc. US., 41: 1079.Google Scholar
7. Turpin, R., Lejeune, J., Lafourcade, J., Chigot, P. L. & Salmon, C., 1961: Présomption de monozygotisme en dépit d'un dimorphisme sexuel: sujet masculin Xy, et sujet neutre haplo X. C. R. Acad. Sc. Paris, 252: 2945.Google Scholar