Abstract
Noncompaction cardiomyopathy (NCCM) is genetically heterogeneous cardiomyopathy with a variable clinical presentation. The prognosis ranges from asymptomatic disease to severe, disabling, progressive heart failure. However, the prevalence, histo-pathological and molecular base of this yet rare, orphan disease is largely unknown. Strategies to improve the accurate diagnosis and outcome should come from large prospective international registries and randomized-controlled trials.
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Caliskan, K., Soliman, O.I., ten Cate, F.J. (2019). Future Perspectives. In: Caliskan, K., Soliman, O., ten Cate, F. (eds) Noncompaction Cardiomyopathy. Springer, Cham. https://doi.org/10.1007/978-3-030-17720-1_10
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DOI: https://doi.org/10.1007/978-3-030-17720-1_10
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