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Malformations Complexes des Membres Supérieurs Associées à une Cardiopathie Congénitale. À propos de six observations

Published online by Cambridge University Press:  01 August 2014

I. Emerit ,
J. de Grouchy ,
M. Laval-Jeantet ,
P. Corone  and
P. Vernant
I. Emerit
Affiliation:
Chaire de Cardiologie, Hôpital Broussais, Chaire de Génétique Médicale Hôpital des Enfants Malades, Service Central de Radiologie Hôpital Broussais - Paris (France)
J. de Grouchy
Affiliation:
Chaire de Cardiologie, Hôpital Broussais, Chaire de Génétique Médicale Hôpital des Enfants Malades, Service Central de Radiologie Hôpital Broussais - Paris (France)
M. Laval-Jeantet
Affiliation:
Chaire de Cardiologie, Hôpital Broussais, Chaire de Génétique Médicale Hôpital des Enfants Malades, Service Central de Radiologie Hôpital Broussais - Paris (France)
P. Corone
Affiliation:
Chaire de Cardiologie, Hôpital Broussais, Chaire de Génétique Médicale Hôpital des Enfants Malades, Service Central de Radiologie Hôpital Broussais - Paris (France)
P. Vernant
Affiliation:
Chaire de Cardiologie, Hôpital Broussais, Chaire de Génétique Médicale Hôpital des Enfants Malades, Service Central de Radiologie Hôpital Broussais - Paris (France)

Summary

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The authors report on six patients exhibiting a congenital heart disease and malformations of the upper limbs. In two of them this association is similar to that described by Holt and Oram in 1960: atrial septal defect, heart arrythmia and abnormal thumbs. The other four patients have the same skeletal anomalies but different heart malformations. Dermatoglyphic studies revealed a high frequency of a distal position of the axial triradius and of an equivalent of a simian crease. The karyotypes are all normal. The etiology is discussed.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 14 , Issue 2 , April 1965 , pp. 132 - 163
Copyright
Copyright © The International Society for Twin Studies 1965

References

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