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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

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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

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