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[Importance of inheritance in cardiomyopathies (author's transl)].

作者信息

Kuhn E

出版信息

Klin Wochenschr. 1977 Jul 15;55(14):673-5. doi: 10.1007/BF01478833.

DOI:10.1007/BF01478833
PMID:895006
Abstract

Inheritance plays an important role in the cardiomyopathies (i.e. dysfunction of the cardiac muscle of unknown origin). This especially has become obvious for the entity asymmetric septal hypertrophy of autosomal dominant inheritance (ASH), a cardiomyopaty with and without obstruction. But this is not the only type of cardiomyopathy of dominant transmittance as was shown by the demonstration of a kindred, in which echocardiographically no hypertrophy of the septum could be found. For it was not possible to find a uniformity for all the affected members of the kindred, for example a congestive course of the disease. Therefore it is suggested to name the disease without any prejudice "cardiomyopathy without asymmetric septal hypertrophy of dominant inheritance" to distinguish it from the "cardiomyopathy with asymetric septal hypertrophy of dominant inheritance". There also may occur a cardiomyopathy of autosomal recessive inheritance. This form could represent a large part of the "sporadic" cardiomyopathies and should challenge to search intensively for enzyme defects as a cause of the disease.

摘要

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引用本文的文献

1
[Familial coincidence of hypertrophic cardiomyopathies and thyroxine-binding globulin deficiency (athyropexinemia) (author's transl)].肥厚型心肌病与甲状腺素结合球蛋白缺乏症(甲状腺素结合球蛋白血症)的家族性巧合(作者译)
Klin Wochenschr. 1978 Dec 15;56(24):1213-6. doi: 10.1007/BF01477077.

本文引用的文献

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Asymmetric septal hypertrophy (ASH): the unifying link in the IHSS disease spectrum. Observations regarding its pathogenesis, pathophysiology, and course.不对称性室间隔肥厚(ASH):特发性肥厚性主动脉瓣下狭窄疾病谱中的统一联系。关于其发病机制、病理生理学及病程的观察
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