Clinical cardiogenetics [electronic resource] / Hubert F. Baars, Pieter A. F. M. Doevendans, Arjan C. Houweling, J. Peter van Tintelen, editors.

This thoroughly revised third edition provides a comprehensive grounding on hereditary heart diseases with special emphasis on the genetic aspects of these conditions. It continues to provide the expertise that all cardiologists, clinical and molecular geneticists, and related medical professionals...

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Bibliographic Details
Online Access: Full Text (via Springer)
Other Authors: Baars, H. F., Doevendans, Pieter A., Houweling, Arjan C., Tintelen, J. Peter van (Johannes Peter), 1964-
Format: Electronic eBook
Language:English
Published: Cham, Switzerland : Springer, 2020.
Edition:3rd ed.
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Summary:This thoroughly revised third edition provides a comprehensive grounding on hereditary heart diseases with special emphasis on the genetic aspects of these conditions. It continues to provide the expertise that all cardiologists, clinical and molecular geneticists, and related medical professionals require to provide optimal care for patients with cardiac disease of genetic origin and for their relatives. Topics covered include the different cardiomyopathies, the primary arrhythmia syndromes and the hereditary thoracic aortic disorders. In addition other topics such as cardiac involvement in hereditary neuromuscular diseases, the clinical policy for sudden cardiac death and the possibilities of pre-implantation genetic diagnosis are included to extend the discussion. Clinical Cardiogenetics compiles current knowledge on the topic in an easy to understand reference. It provides a practical clinical primer for cardiologists, clinical geneticists, trainees and other physicians involved in the management of these patients.
Physical Description:1 online resource : illustrations.
Bibliography:References -- 2: Clinical Genetics -- Introduction -- The Clinical Genetic Intake -- Family History -- Pedigree Construction -- Basic Concepts in Inherited Disease -- Mitosis and Meiosis -- Chromosomal Abnormalities -- Inheritance Patterns -- Single-Gene Disorders: Mendelian Inheritance -- Autosomal Dominant Inheritance -- Autosomal Recessive Inheritance -- X-Linked Recessive Inheritance -- X-Linked Dominant Inheritance -- Non-Mendelian Inheritance -- Multifactorial Inheritance -- Maternal (Mitochondrial) Inheritance -- New (De Novo) Mutations -- Mosaicism.
ISBN:9783030454579
3030454576