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On the gene-carriers of Fuchs' atrophia gyrata chorioideae et retinae

Published online by Cambridge University Press:  01 August 2014

J. François ,
F. Barbier  and
A. De Rouck
J. François
Affiliation:
Clinique Ophtalmologique de l'Université de Gand (Belgique)
F. Barbier
Affiliation:
Clinique Ophtalmologique de l'Université de Gand (Belgique)
A. De Rouck
Affiliation:
Clinique Ophtalmologique de l'Université de Gand (Belgique)

Summary

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Alder's anomaly of the leucocytes, which had been considered as a manifestation of the gene-carrier of Fuchs' atrophia gyrata chorioideae et retinae, has not been found in other cases of the latter disease.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 15 , Issue 1 , January 1966 , pp. 34 - 35
Copyright
Copyright © The International Society for Twin Studies 1966

References

Bibliographie

François, J. et al. (1960). Les conducteurs du gène de l'atrophia gyrata chorioideae et retinae de Fuchs (anomalie d'Aider). A.Ge.Me.Ge. 9: 74–90.Google Scholar
Kurstjens, J.H. (1965). Choroideremia and gyrate atrophy of the choroid and retina. Doc. Ophthal., 19: 1–122.CrossRefGoogle Scholar