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https://thefhfoundation.org/fh-family-support-group
FH Family Support Group. Familial Hypercholesterolemia (FH) is an inherited disorder of cholesterol metabolism leading to premature coronary heart disease. 1 in 500 West Australians have FH but 80% of cases are not diagnosed. The early diagnosis and treatment of FH can delay or prevent the onset of Coronary Heart Disease.
https://ghr.nlm.nih.gov/condition/familial-hypercholesterolemia
Familial hypercholesterolemia is an inherited condition characterized by very high levels of cholesterol in the blood. Cholesterol is a waxy, fat-like substance that is produced in the body and obtained from foods that come from animals (particularly egg yolks, meat, poultry, fish, and dairy products).
https://rarediseases.info.nih.gov/diseases/10416/disease
Jun 18, 2015 · Familial hypercholesterolemia is a condition characterized by very high levels of cholesterol in the blood due to mutations in the LDLR gene.People with hypercholesterolemia have a high risk of developing a form of heart disease called coronary artery disease, as well as health problems related to the buildup of excess cholesterol in other tissues (e.g., in the tendons and skin).
https://www.accredo.com/conditions/familial_hypercholesterolemia
What is familial hypercholesterolemia. Familial hypercholesterolemia (FH) is a rare genetic disorder that involves extremely high amounts of cholesterol in the blood, especially low-density lipoprotein (LDL). Because high LDL is one of many risk factors associated with heart disease, LDL is …
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4472364/
Familial hypercholesterolemia is a common, inherited disorder of cholesterol metabolism that leads to early cardiovascular morbidity and mortality. It is underdiagnosed and undertreated. Statins, ezetimibe, bile acid sequestrants, niacin, lomitapide, mipomersen and LDL apheresis are treatments that can lower LDL cholesterol levels.
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