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EARLY DETECTION OF A PATIENT WITH FAMILY HYPERTRIGLYCERIDEMIA BY TELEMEDICINE LABORATORY PROGRAM

T. Arrobas Velilla, R. Gonzalez Moreno,M. J. Ariza Corbo,M. A. Rico Corral,J. Rioja Villodres,P. Valdivielso Felices

Atherosclerosis（2021）

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Abstract
Background and Aims: Familial hypertriglyceridaemia is an autosomal dominant disorder of lipid metabolism with an incidence around 0.5-1% characterized by elevated triglyceride due to a mutation in the gene that encodes ApoA-5.
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