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Genetik in der Reproduktionsmedizin

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Reproduktionsmedizin

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Zusammenfassung

Störungen der Fertilität haben bei Frauen und Männern häufig hereditäre Ursachen. Das Spektrum möglicher genetischer Veränderungen ist dabei weit. Es reicht von Chromosomenaberrationen, die in klassischen zytogenetischen Untersuchungen erkannt werden können, über Mikrodeletionen hin zu verschiedenen monogenen Erkrankungen. Fertilitätsstörungen können ferner auch als Teilsymptom bei vielen übergeordneten syndromalen Krankheitsbildern auftreten.

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Authors and Affiliations

  1. Institut für Humangenetik, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Deutschland

    G. Gillessen-Kaesbach & Y. Hellenbroich

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  1. G. Gillessen-Kaesbach
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  2. Y. Hellenbroich
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Correspondence to G. Gillessen-Kaesbach .

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Editors and Affiliations

  1. Facharzt-Zentrum für Kinderwunsch, Pränatale Medizin, Endokrinologie und Osteologie Hamburg GmbH, amedes experts, Hamburg, Germany

    Klaus Diedrich

  2. SYNLAB Holding Deutschland GmbH, Augsburg, Hamburg, Germany

    Michael Ludwig

  3. Sektion für gynäkologische Endokrinologie und Reproduktionsmedizin, UNIVERSITÄTSKLINIKUM Schleswig-Holstein – Campus Lübeck, Lübeck, Schleswig-Holstein, Germany

    Georg Griesinger

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Gillessen-Kaesbach, G., Hellenbroich, Y. (2018). Genetik in der Reproduktionsmedizin. In: Diedrich, K., Ludwig, M., Griesinger, G. (eds) Reproduktionsmedizin. Springer Reference Medizin. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-55601-6_45-1

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  • DOI: https://doi.org/10.1007/978-3-662-55601-6_45-1

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  • Print ISBN: 978-3-662-55601-6

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