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Genetic Counseling in Congenital Deafness

Published online by Cambridge University Press:  01 August 2014

J. François ,
S. De Bie  and
M.Th. Matton-Van Leuven
J. François*
Affiliation:
Département de Génétique Médicale de la, Clinique Ophtalmologique de l'Université de Gand, Belgique
S. De Bie
Affiliation:
Département de Génétique Médicale de la, Clinique Ophtalmologique de l'Université de Gand, Belgique
M.Th. Matton-Van Leuven
Affiliation:
Département de Génétique Médicale de la, Clinique Ophtalmologique de l'Université de Gand, Belgique
*
Département de Génétique Médicale, Clinique Ophtalmologique de l'Université, De Pintelaan 135, B-9000 Gand, Belgique

Abstract

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The risk of having a child affected by isolated congenital deafness (or deafmutism) is high, if the two parents are affected, if only one parent is affected, but belonging to an affected family, and if the couple has already an affected child.

Résumé

RÉSUMÉ

Le risque d'avoir un enfant atteint de surdité congénitale isolée (ou de surdi-mutité) est élevé, si les deux parents sont atteints, si un seul parent est atteint, mais constitue un cas familial, et si le couple a déjà un enfant atteint.

Riassunto

RIASSUNTO

Il rischio di avere un figlio affetto da sordità congenita isolata (o sordomutismo) è elevato se i due genitori sono affetti, oppure se è affetto un solo genitore che però proviene da una famiglia affetta, o infine se la coppia ha già avuto un figlio affetto.

Zusammenfassung

ZUSAMMENFASSUNG

Die Wahrscheinlichkeit eines Kindes mit angeborener isolierter Taubheit (oder Taubstummheit) ist sehr gross, wenn beide Eltern daran leiden, wenn nur ein Elternteil daran leidet, in dessen Familie das Leiden jedoch vorgekommen ist oder wenn die Eltern bereits ein taubes oder taubstummes Kind hatten.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 24 , Issue 3-4 , 07-10 1975 , pp. 295 - 297
Copyright
Copyright © The International Society for Twin Studies 1975

References

BIBLIOGRAPHIE

Chung, C.S., Robinson, O.W., Morton, N.E. 1969. A note of deaf-mutism. Ann. Hum. Genet., 23: 357–366.Google Scholar
Deraemaeker, R. 1972. Erfelijke congenitale doofheid in de provincie Antwerpen. Tijdschr. Genee-skunde, 28: 496–505.Google Scholar
Fraser, G.R. 1964. Profound childhood deafness. J. Med. Genet., 1: 118–151.Google Scholar
Murphy, E.A. 1973. Probabilities in genetic counselling. In: Contemporary Genetic Counselling. Birth Defects, 9: 19–33.Google Scholar
Sank, D. 1963. Genetic aspects of early total deafness. In: Family and Mental Health Problems in a Deaf Population [pp. 28–81]. New York: Columbia University Press.Google Scholar
Stevenson, A.C., Davison, B.C.C. 1970. Genetic Counselling. London: William Heineman Medical Books Limited.Google Scholar