What is another word for Familial Combined Hyperlipidemia?
Pronunciation: [famˈɪlɪəl kəmbˈa͡ɪnd hˌa͡ɪpəlˌɪpa͡ɪdˈiːmi͡ə] (IPA) 
Familial combined hyperlipidemia is a genetic disorder characterized by an abnormal increase in cholesterol and triglyceride levels in the blood. This condition is often referred to by other terms, including "familial combined hyperlipoproteinemia" and "familial dyslipidemia". These alternative synonyms highlight the fundamental nature of the disorder, primarily affecting lipids (fats) in the bloodstream due to familial or inheritable factors. While the precise terminology may differ, it is important to understand that all these synonyms refer to the same condition, highlighting the genetic predisposition, the combination of lipids involved, and the resulting health implications. Early diagnosis and appropriate management are essential for individuals with familial combined hyperlipidemia to prevent potential complications related to cardiovascular health.
