Background. Inherited heart disease is becoming a substantial part of everyday cardiology practice while genetic counselling still only takes place at university hospitals. In this study we review our seven-year experience with cardiogenetic counselling in a non-university hospital. Methods. Retrospective analysis of patient records. Results. A total number of 83 index patients were counselled. In 65 patients DNA tests were performed, resulting in 26 positive tests. In all patients with genotype confirmation of hereditary cardiovascular disease and in 32 families without a molecular diagnosis, family screening was advised. Out of 120 subsequently tested family members, 47 molecular genetic diagnoses were confirmed. Conclusion. Although the ...
International audienceAims: Cardiomyopathies comprise a heterogeneous group of diseases, often of ge...
Abstract Background The diagnostic yield of genetic testing for inherited cardiac diseases is up to ...
Increasing numbers of patient relatives at risk of developing dilated or hypertrophic cardiomyopathy...
Background. Inherited heart disease is becoming a substantial part of everyday cardiology practice w...
During the past decade, developments in the field of DNA diagnostics have resulted in the confirmati...
Introduction: We evaluated the results of 15 years of cardiogenetic counseling in the Academic Medic...
Introduction: We evaluated the results of 15 years of cardiogenetic counseling in the Academic Medic...
The underlying genetic etiologies for a group of conditions known as inherited cardiac disease are b...
The introduction of next-generation sequencing in everyday clinical genetics practise is increasing ...
Aims: Cardiomyopathies comprise a heterogeneous group of diseases, often of genetic origin. We asses...
The introduction of next-generation sequencing in everyday clinical genetics practise is increasing ...
Hypertrophic cardiomyopathy (HCM) is a common hereditary heart disease associated with sudden cardia...
In recent years, the importance of genetic causes of cardiovascular diseases has been increasingly r...
Developments in DNA-diagnostic techniques allow us to identify a significant proportion of patients ...
Increasing numbers of patient relatives at risk of developing dilated or hypertrophic cardiomyopathy...
International audienceAims: Cardiomyopathies comprise a heterogeneous group of diseases, often of ge...
Abstract Background The diagnostic yield of genetic testing for inherited cardiac diseases is up to ...
Increasing numbers of patient relatives at risk of developing dilated or hypertrophic cardiomyopathy...
Background. Inherited heart disease is becoming a substantial part of everyday cardiology practice w...
During the past decade, developments in the field of DNA diagnostics have resulted in the confirmati...
Introduction: We evaluated the results of 15 years of cardiogenetic counseling in the Academic Medic...
Introduction: We evaluated the results of 15 years of cardiogenetic counseling in the Academic Medic...
The underlying genetic etiologies for a group of conditions known as inherited cardiac disease are b...
The introduction of next-generation sequencing in everyday clinical genetics practise is increasing ...
Aims: Cardiomyopathies comprise a heterogeneous group of diseases, often of genetic origin. We asses...
The introduction of next-generation sequencing in everyday clinical genetics practise is increasing ...
Hypertrophic cardiomyopathy (HCM) is a common hereditary heart disease associated with sudden cardia...
In recent years, the importance of genetic causes of cardiovascular diseases has been increasingly r...
Developments in DNA-diagnostic techniques allow us to identify a significant proportion of patients ...
Increasing numbers of patient relatives at risk of developing dilated or hypertrophic cardiomyopathy...
International audienceAims: Cardiomyopathies comprise a heterogeneous group of diseases, often of ge...
Abstract Background The diagnostic yield of genetic testing for inherited cardiac diseases is up to ...
Increasing numbers of patient relatives at risk of developing dilated or hypertrophic cardiomyopathy...