Two Families of Familial Cardiomegaly with a Proved Consanguinity
نویسندگان
چکیده
منابع مشابه
[Familial cardiomegaly].
In 1949 William Evans gave the name of familial cardiomegaly to what he believed to be a "distinct syndrome having a definite clinical, cardiographic, and pathological pattern." The essential features were the familial incidence of cardiomegaly without obvious cause and a marked tendency to arrhythmia and heart block with associated palpitation, giddiness, and syncope. Death may be sudden or ra...
متن کاملFamilial cardiomegaly.
In 1949 William Evans gave the name of familial cardiomegaly to what he believed to be a "distinct syndrome having a definite clinical, cardiographic, and pathological pattern." The essential features were the familial incidence of cardiomegaly without obvious cause and a marked tendency to arrhythmia and heart block with associated palpitation, giddiness, and syncope. Death may be sudden or ra...
متن کاملFamilial idiopathic cardiomegaly.
AMONG CAUSES of cardiac enlargement Of obscure origin that confront the clinician and pathologist alike are subendocardial fibroelastosis, inflammatory myocardiopathies, glycogen-storage disease, amyloidosis, muscular subaortic stenosis,' asymmetrical hypertrophy of the heart,2 idiopathic myocardiopathy,3 and familial cardiomegaly. Familial cardiomegaly, originally named in 1949 by Evans,4 has ...
متن کاملFamilial Idiopathic Cardiomegaly By WAYNE
AMONG CAUSES of cardiac enlargement Of obscure origin that confront the clinician and pathologist alike are subendocardial fibroelastosis, inflammatory myocardiopathies, glycogen-storage disease, amyloidosis, muscular subaortic stenosis,' asymmetrical hypertrophy of the heart,2 idiopathic myocardiopathy,3 and familial cardiomegaly. Familial cardiomegaly, originally named in 1949 by Evans,4 has ...
متن کاملPractice of Consanguinity and Unusual Cases of Inherited Familial Chromosome Abnormalities: A Case Report
We present 2 cases of likely rare event. In case 1, 3rd degree consanguineous marriage revealed inv(6) with same break points in parents who were found to be phenotypically normal. The same inv(6) being inherited in progeny but presented with low AMH (anti Mullerian hormone) and high level of FSH (follicular stimulating hormone) leading to polycystic ovarian syndrome/premature ovarian failure. ...
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ژورنال
عنوان ژورنال: Japanese Circulation Journal
سال: 1967
ISSN: 0047-1828,1347-4839
DOI: 10.1253/jcj.31.885