Cardiac complications in inherited mitochondrial diseases
作者： Mohaddeseh Behjati , Mohammad Reza Sabri , Masood Etemadi Far , Majid Nejati
DOI: 10.1007/S10741-020-10009-1
关键词:
摘要: Maternally mitochondrial dysfunction includes a heterogeneous group of genetic disorders which leads to the impairment final common pathway energy metabolism. Coronary heart disease and coronary venous are two important clinical manifestations due abnormality in setting underlying pathways. Mitochondrial can lead cardiomyopathy, is involved onset acute cardiac pulmonary failure. diseases present other such as left ventricular noncompaction conduction disease. Different findings from originate different mtDNA mutations, this variety symptoms poses diagnostic challenge for cardiologists. Heart transplantation may be good treatment, but it not always possible, complications disease, encephalopathy, lactic acidosis, stroke-like syndrome, should considered. To diagnose treat most disorders, careful cardiac, neurological, molecular studies needed. In study, we looked at genetics MIDs patients with dysfunction.
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