Titlebook: Clinical Cardiogenetics; Hubert F. Baars,Pieter A. F. M. Doevendans,J. Pete Book 20162nd edition Springer International Publishing Switzer

子女

https://doi.org/10.1007/978-3-658-08575-9ardiomyopathies, muscular dystrophy, or syndromic disease, perturb a diverse set of important myocardial proteins to produce a final DCM phenotype. Recommendations on genetic screening and cardiac screening are provided in this chapter.

包庇

https://doi.org/10.1007/978-3-658-39621-3e-corrected QT interval (QTc) on the surface electrocardiogram (ECG). This chapter reviews the clinical presentation of LQTS, its diagnosis, and principles of management in the context of recent clinical advances and molecular genetics, with a focus on the most common forms of LQTS – LQT1, LQT2, and LQT3.

持续

Clinical Genetics familial diseases. Both are specifically trained in communicating the implications of genetic information and genetic disease to patients and their families. Clinical geneticists and genetic counsellors often work together with cardiologists to ensure a high standard of care for families with cardiogenetic diseases.

跳脱衣舞的人

Dilated Cardiomyopathyardiomyopathies, muscular dystrophy, or syndromic disease, perturb a diverse set of important myocardial proteins to produce a final DCM phenotype. Recommendations on genetic screening and cardiac screening are provided in this chapter.

Fretful

RODE

亲密

吹牛者

Book 20162nd editionh a genetic disease. With detailed discussion of the basic science of cardiogenetics in order to assist in the clinical understanding of the topic.. . .The genetic causes of various cardiovascular diseases are explained in a concise clinical way that reinforces the current management doctrine in a p

Decongestant

Hans-Jürgen Siegert,Siegfried Bocioneking the correct etiology, guiding patient management and directing family screening. In this chapter, we discuss the differential diagnosis of CCD, guiding principles in cardiogenetic evaluation as well as specific genotype-phenotype correlations.

Encoding

Hereditary Cardiac Conduction Diseasesing the correct etiology, guiding patient management and directing family screening. In this chapter, we discuss the differential diagnosis of CCD, guiding principles in cardiogenetic evaluation as well as specific genotype-phenotype correlations.