Hypercholesterolemia causes: Difference between revisions
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*[[Alagille syndrome]] | *[[Alagille syndrome]] |
Latest revision as of 21:17, 10 January 2020
Hyperlipoproteinemia Microchapters |
ACC/AHA Guideline Recommendations |
Intensity of statin therapy in primary and secondary prevention |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Luke Rusowicz-Orazem, B.S.
Overview
Hypercholesterolemia is primarily caused by cardiovascular conditions resulting from lifestyle, renal disease, and congenital conditions.
Causes
Common Causes
- Abetalipoproteinemi
- Alagille syndrome
- ApoA1 deficiency
- Apob mutation
- Apolipoprotein c-ii deficiency
- Apoprotein e deficiency
- Beckwith-wiedemann syndrome
- Beta blockers
- Carbohydrate intake
- Cholestatic jaundice
- Chronic renal insufficiency
- Ciclosporin
- Cushing’s syndrome
- Diabetes mellitus
- Diabetes mellitus type 2
- Dialysis
- Familial defective apolipoprotein b-100
- Familial mixed hyperlipidaemia
- Hypothyroidism
- Idiopathic
- Lack of exercise
- Lack of physical activity
- Ldl receptor deficiency
- Ldlr mutation
- Ldlrap1 mutation
- Lipoprotein lipase deficiency
- Malignant hepatopathy
- Metabolic syndrome
- Monoclonal gammopathy
- Nephrotic syndrome
- Obesity
- Obstructive liver disease
- Oculomotor apraxia syndrome
- Pcsk9 mutation
- Tobacco
- Trans fatty acids
- Vitamin e deficiency
Causes by Organ System
Causes in Alphabetical Order
- Abetalipoproteinemia
- Alagille syndrome
- Alcohol
- Alström syndrome
- Analbuminaemia
- Anorexia nervosa
- ApoA1 deficiency
- Apob mutation
- Apolipoprotein c-ii deficiency
- Apoprotein e deficiency
- Beckwith-wiedemann syndrome
- Beta blockers
- Carbohydrate intake
- Carcinoma
- Cholestatic jaundice
- Cholesterol ester storage disease
- Chromosome 14 uniparental disomy syndrome
- Chromosome 3, trisomy 3p
- Chronic renal insufficiency
- Ciclosporin
- Cushing’s syndrome
- Cushing's syndrome
- Diabetes mellitus
- Diabetes mellitus type 2
- Dialysis
- Familial
- Familial defective apolipoprotein b-100
- Familial mixed hyperlipidaemia
- Fosamprenavir
- Glucocorticoids
- Glycogenosis type 1a
- Glycogenosis type 3
- Glycogenosis type 6
- Hypothyroidism
- Idiopathic
- Lack of exercise
- Lack of physical activity
- Ldl receptor deficiency
- Ldlr mutation
- Ldlrap1 mutation
- Lipoprotein lipase deficiency
- Malignant hepatopathy
- Medications
- Metabolic syndrome
- Mitotane
- Monoclonal gammopathy
- Nephrotic syndrome
- Obesity
- Obstructive liver disease
- Oculomotor apraxia syndrome
- Pcsk9 mutation
- Pregnancy
- Retinoic acid
- Siltuximab
- Sirolimus
- Temsirolimus
- Thiazide diuretics
- Tobacco
- Tocilizumab
- Tofacitinib
- Trans fatty acids
- Vitamin e deficiency
- Werner syndrome
- Zieve's syndrome