Hostname: page-component-cd9895bd7-p9bg8 Total loading time: 0 Render date: 2024-12-23T05:13:37.936Z Has data issue: false hasContentIssue false
  • English
  • Français

Quadro Elettroencefalografico in una Famiglia con due Fratelli affetti da Retinopatia Pigmentosa, Ipoacusia, Polidattilia

Published online by Cambridge University Press:  01 August 2014

L. Gedda ,
M. L. Restivo-Manfridi  and
L. Romei
L. Gedda
Affiliation:
Istituto di Genetica Medica e Gemellologia, «G. Mendel», Roma Arcispedale del SS. Salvatore, Roma, Reparto Oculistico
M. L. Restivo-Manfridi
Affiliation:
Istituto di Genetica Medica e Gemellologia, «G. Mendel», Roma Arcispedale del SS. Salvatore, Roma, Reparto Oculistico
L. Romei
Affiliation:
Istituto di Genetica Medica e Gemellologia, «G. Mendel», Roma Arcispedale del SS. Salvatore, Roma, Reparto Oculistico

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 EEG alterations found in two brothers affected by pigmentary retinopathy, syndactilia and hypoacusia, and in their relatives. The EEG resulted to be altered aspecifically in the propositi, in their mother and their two clinically healthy sisters. The father was normal. Reports on EEG alterations in patients with pigmentary retinopathy are rather frequent, while such report is rare in healthy relatives.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 16 , Issue 4 , October 1967 , pp. 350 - 364
Copyright
Copyright © The International Society for Twin Studies 1967

References

Bibliografia

Bardelli, A. M., Verdovini, F. (1960). Arch. Oftal., 64: 283.Google Scholar
Beussart, M. et al. (1959). Corrélation entre les caractères EEG somatiques et psychologiques de 5 couples de jumeaux MZ normaux. Rev. Neurol., 101: 495.Google Scholar
Caldonazzo, C. (1961). Retinite pigmentosa in oligofrenia con epilessia centrocefalica. Rass. Stud. Psichiat., 50: 37.Google Scholar
Cavka, M. V. (1953). Cit. Ford, 1952.Google Scholar
Charters, A. D. (1957). Cit. Ford, 1952.Google Scholar
Cordier, J. et al. (1956). L'électroencéphalogramme au cours des dégénérescences tapéto-rétiniennes. Rev. Oto-Neuro-Ophtal., 28: 193.Google Scholar
Failla, E., Morocutti, C. (1950). Su un caso di retinite pigmentosa associata ad epilessia temporale e a diabete insipido. Acta Neurol., 15: 62.Google Scholar
Ford, F. R. (1952). Diseases of the Nervous System in Infancy, Childhood, and Adolescence. OxFord.Google Scholar
Franceschetti, A., Klein, D. (1947). Cit. François, 1957.Google Scholar
François, J. (1957). L'Heredité en Ophtalmologie. Ed. Masson., Paris.Google Scholar
François, J., Bello, A. (1952). Le syndrome de Laurence-Moon-Bardet-Biedl. Amer. Ocul., 185: 944.Google Scholar
François, J., De Rouck, A. (1957). L'intérêt de l'electro-rétino-encéphalographie dans le diagnostic différentiel des dégénérescences tapéto-rétiniennes. Bull. Soc. Belge. Ophtal., 115: 511.Google Scholar
François, J. ( 1965). Elektroretinographische und elektroenzephalographische Untersuchungen bei der Storgardtschen Erkrankung. Klin. M. Augenheilk., 147: 654.Google Scholar
François, J. et al. (1954). L'électro-rétino-encéphalographie dans la rétinopathie pigmentaire. Ann. Oculist., 187: 808.Google Scholar
Froment, J. et al. (1937). Cit. Ford, 1952.Google Scholar
Gillespie, J. D., Dohoque, V. Z. (1964). Electroencephalograms in retinitis pigmentosa. Amer. J. Ophthal., 57: 1045.Google Scholar
Guiner, J., Bruger, M. (1947). Cit. Ford, 1952.Google Scholar
Hagen, P. B. et al. (1951). Cit. Ford, 1952.Google Scholar
Jayle, G. E. et al. (1953). Constatations électro-encéphalographiques et syndrome de Bardet-Biedl. Bull. Soc. Ophtal. Franc., 81.Google Scholar
Kjerrumgaard, E. (1948). Cit. Ford, 1952.Google Scholar
Krill, A. E., Stamps, E. W. (1960). The electroencephalogram in retinitis pigmentosa. Amer. J. Ophthal., 49: 762.CrossRefGoogle ScholarPubMed
Larmande, A. M., Susini, R. (1952). Données électroencéphalographiques et pathogénie du syndrome de Bardet-Biedl. Soc. Franc. Ophtal., 55: 122.Google Scholar
Lennox, Gibbs. Cit. Beaussart et al. Google Scholar
Morocutti, C., Vanni, V. (1959). Cit. Gillespie, 1964.Google Scholar
Stewart, R. M. (1937). Cit. Ford, 1952.Google Scholar
Streifler, M., Landau, J. (1955). Electrical brain potential in retinitis pigmentosa and familial hemeralopia. Ophtalmologica, 130: 116.Google Scholar
Von Stock, W. (1908). Cit. Ford, 1952.Google Scholar