Since 2020 arrhythmogenic cardiomyopathy includes a right dominant form, a biventricular form and a left dominant form. Already in 2004 Carvajal syndrome was first described in Ecuador within families [1]. This syndrome includes a slighty dilated, poor contracting left ventricle and hair and skin abnormalities with curly hair and plantopalmar keratosis. The genetic background were mutations of the desmoplakin gene.
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Stefan Peters (2024) studied this question.
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