Key result
Skin features in inherited desmosomal cardiocutaneous syndromes may serve as early hallmarks for progressive and potentially lethal cardiac disease, providing opportunities for early intervention.
Skin features in desmosomal cardiocutaneous syndromes may serve as early hallmarks for progressive and potentially lethal cardiac disease, allowing for early recognition and intervention.
May flag cardiac risk via skin exam in desmosomal syndromes; leaves open whether screening improves outcomes.
Both skin and heart are subject to shear mechanical stress and need to be stress-resistant in a flexible way. The intercellular connecting structures in skin and heart, the desmosomes, that have to resist these forces show remarkable resemblance in epidermis and myocardium. Mutations in desmosomal proteins lead to inherited desmosomal cardiocutaneous syndromes (DCCS): une liaison dangereuse. This article will critically review the cutaneous and cardiac features as well as the molecular background of DCCS, such as Naxos disease and Carvajal syndrome caused by deficiencies of plakoglobin and desmoplakin respectively. In addition, potential other desmosomal gene candidates for an involvement in cardiocutaneous syndromes are considered. The skin features in these syndromes may be the hallmark for the presence of progressive and ultimately lethal cardiac disease. Knowledge of these skin features and early recognition of such a syndrome may provide opportunities to halt or slow down cardiac disease progression, treat arrhythmias and even prevent sudden death.
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Bolling et al. (2009) conducted a review in Inherited desmosomal cardiocutaneous syndromes (DCCS). Desmosomal cardiocutaneous syndromes (DCCS) was evaluated. Skin features in inherited desmosomal cardiocutaneous syndromes may serve as early hallmarks for progressive and potentially lethal cardiac disease, providing opportunities for early intervention.
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