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Cardiomyopathies in Women

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Manual of Gynecardiology

Abstract

Peripartum cardiomyopathy (PPCM) is a potentially threatening disease in low and middle income countries, where healthcare systems and supervision during pregnancy are not well controlled and doctors are unaware of the disease. Symptoms and signs are typical for systolic HF and may develop rapidly, leading to severe acute systolic failure, ventricular arrhythmias or sudden cardiac death. Inhibiting prolactin secretion with Bromocriptine may offer a novel specific therapeutic option. Dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM), and probably also non-compaction and arrhythmogenic right ventricular CM have a greater prevalence in men than in women. This chapter contains expert information on sex differences in myocardial adaptation of the human heart.

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Acknowledgement

I thank Arne Kühne for excellent management of the references and Martina Rudek and Sarah Lisa Müller for editorial support. The work was supported by grants from DZHK and from EU FP 7 (RADOX and EUGenMed).

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Correspondence to Vera Regitz-Zagrosek M.D., Ph.D. .

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Regitz-Zagrosek, V., Hilfiker-Kleiner, D., Pfeffer, T. (2017). Cardiomyopathies in Women. In: Maas, A., Bairey Merz, C. (eds) Manual of Gynecardiology. Springer, Cham. https://doi.org/10.1007/978-3-319-54960-6_8

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  • DOI: https://doi.org/10.1007/978-3-319-54960-6_8

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