High cholesterol causes: Difference between revisions
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{{col-begin|width=80%}} | {{col-begin|width=80%}} | ||
{{col-break|width=33%}} | {{col-break|width=33%}} | ||
*[[Apo A-I deficiency]] | *[[Apo A-I deficiency]] | ||
*[[Berardinelli–Seip syndrome]] | *[[Berardinelli–Seip syndrome]] | ||
*[[Diabetes mellitus]] | *[[Diabetes mellitus]] | ||
*[[Alcoholism]] | *[[Alcoholism]] | ||
*[[Hypothyroidism]] | *[[Hypothyroidism]] | ||
*[[IgA nephropathy ]] | *[[IgA nephropathy ]] | ||
*[[Hashimoto's thyroiditis ]] | *[[Hashimoto's thyroiditis ]] | ||
*[[Metabolic syndrome ]] | *[[Metabolic syndrome ]] | ||
*[[Alagille syndrome]] | *[[Alagille syndrome]] | ||
*[[Alström syndrome]] | *[[Alström syndrome]] | ||
*[[Analbuminaemia]] | *[[Analbuminaemia]] | ||
*[[Antiretroviral therapy]] | *[[Antiretroviral therapy]] | ||
*[[Apolipoprotein B deficiency]] | *[[Apolipoprotein B deficiency]] | ||
*[[Apolipoprotein C2|Apolipoprotein C2 deficiency]] | *[[Apolipoprotein C2|Apolipoprotein C2 deficiency]] | ||
*[[Apolipoprotein E|Apoliprotein E deficiency]] | *[[Apolipoprotein E|Apoliprotein E deficiency]] | ||
*[[Familial hypercholesterolemia|Autosomal recessive hypercholesterolemia]] | *[[Familial hypercholesterolemia|Autosomal recessive hypercholesterolemia]] | ||
*[[Beta blockers]] | *[[Beta blockers]] | ||
{{col-break|width=33%}} | {{col-break|width=33%}} | ||
*[[Binge eating disorder]] | *[[Binge eating disorder]] | ||
*[[Chronic kidney disease]] | *[[Chronic kidney disease]] | ||
*[[Corticosteroids]] | |||
*[[Corticosteroids]] | |||
*[[Cyclosporine]] | *[[Cyclosporine]] | ||
*[[Estrogens]] | *[[Estrogens]] | ||
*[[Everolimus]] | |||
*[[Everolimus]] | |||
*[[Familial combined hyperlipidemia]] | *[[Familial combined hyperlipidemia]] | ||
*[[Familial hypercholesterolemia]] | *[[Familial hypercholesterolemia]] | ||
*[[Fosamprenavir]] | *[[Fosamprenavir]] | ||
*[[Glycogen storage disease type 1a]] | *[[Glycogen storage disease type 1a]] | ||
*[[Glycogenosis type 3]] | |||
*[[Glycogenosis type 3]] | |||
*[[Glycogenosis type 6]] | *[[Glycogenosis type 6]] | ||
*[[Hyperlipoproteinemia|Familial hyperlipoproteinemia type 5]] | *[[Hyperlipoproteinemia|Familial hyperlipoproteinemia type 5]] | ||
*[[Hypothyroidism]] | *[[Hypothyroidism]] | ||
*[[Lecithin cholesterol acyltransferase deficiency]] | *[[Lecithin cholesterol acyltransferase deficiency]] | ||
*[[Lipoprotein lipase deficiency]] | |||
*[[Lipoprotein lipase deficiency]] | |||
*[[Mitotane]] | *[[Mitotane]] | ||
{{col-break|width=33%}} | {{col-break|width=33%}} | ||
*[[Nephrotic syndrome]] | *[[Nephrotic syndrome]] | ||
*[[Niemann-Pick disease type B]] | *[[Niemann-Pick disease type B]] | ||
*[[Obesity]] | |||
*[[Obesity]] | *[[Olanzapine]] | ||
*[[Olanzapine]] | |||
*[[Polycystic ovary syndrome]] | *[[Polycystic ovary syndrome]] | ||
*[[Pregnancy]] | *[[Pregnancy]] | ||
*[[Primary biliary cirrhosis]] | |||
*[[Primary biliary cirrhosis]] | |||
*[[Sirolimus]] | *[[Sirolimus]] | ||
*[[Stauffer syndrome]] | *[[Stauffer syndrome]] | ||
*[[Tamoxifen ]] | *[[Tamoxifen ]] | ||
*[[Temsirolimus]] | *[[Temsirolimus]] | ||
*[[Thiazide diuretics]] | |||
*[[Thiazide diuretics ]] | |||
*[[Tocilizumab]] | *[[Tocilizumab]] | ||
*[[Tofacitinib]] | *[[Tofacitinib]] | ||
*[[Werner syndrome]] | |||
*[[Werner syndrome]] | |||
*[[Zieve's syndrome]] | *[[Zieve's syndrome]] | ||
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|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Drug Side Effect''' | | '''Drug Side Effect''' | ||
|bgcolor="Beige"| [[Antiretroviral therapy]], [[Beta blockers]], [[Corticosteroids]], [[Cyclosporine]], [[Estrogens]], [[Everolimus]], [[Fosamprenavir]], [[Mitotane]], [[Olanzapine]], [[Sirolimus]], [[Tamoxifen ]], [[Temsirolimus]],[Thiazide diuretics ]], [[Tocilizumab]], [[Tofacitinib]] | |bgcolor="Beige"| [[Antiretroviral therapy]], [[Beta blockers]], [[Corticosteroids]], [[Cyclosporine]], [[Estrogens]], [[Everolimus]], [[Fosamprenavir]], [[Mitotane]], [[Olanzapine]], [[Sirolimus]], [[Tamoxifen ]], [[Temsirolimus]], [[Thiazide diuretics]], [[Tocilizumab]], [[Tofacitinib]] | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
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|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Endocrine''' | | '''Endocrine''' | ||
|bgcolor="Beige"| [[ | |bgcolor="Beige"| [[Metabolic syndrome]], [[Metabolic syndrome]], [[Polycystic ovary syndrome]], [[Werner syndrome]] | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
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|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Gastroenterologic''' | | '''Gastroenterologic''' | ||
|bgcolor="Beige"| [[Glycogenosis type 6]], [[Niemann-pick disease | |bgcolor="Beige"| [[Glycogenosis type 6]], [[Niemann-pick disease type B ]], [[Primary biliary cirrhosis]], [[Stauffer syndrome]], [[Zieve's syndrome]] | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Genetic''' | | '''Genetic''' | ||
|bgcolor="Beige"|[[Apo A-I deficiency]], [[Apolipoprotein b deficiency ]], [[Apolipoprotein | |bgcolor="Beige"|[[Apo A-I deficiency]], [[Apolipoprotein b deficiency ]], [[Apolipoprotein C2|Apolipoprotein C2 deficiency]], [[Apoliprotein E|Apoliprotein E deficiency]], [[Familial hypercholesterolemia|Autosomal recessive hypercholesterolemia]], [[Familial combined hyperlipidemia]], | ||
[[Familial hypercholesterolemia]], [[Glycogen storage disease type 1a]], [[Glycogenosis type 3]], [[Glycogenosis type 6]], [[Hyperlipoproteinemia|Familial hyperlipoproteinemia type 5]], [[Lecithin cholesterol acyltransferase deficiency]], [[Lipoprotein lipase deficiency]], [[Niemann-pick disease type B]], [[Werner syndrome]] | [[Familial hypercholesterolemia]], [[Glycogen storage disease type 1a]], [[Glycogenosis type 3]], [[Glycogenosis type 6]], [[Hyperlipoproteinemia|Familial hyperlipoproteinemia type 5]], [[Lecithin cholesterol acyltransferase deficiency]], [[Lipoprotein lipase deficiency]], [[Niemann-pick disease type B]], [[Werner syndrome]] | ||
|- | |- |
Revision as of 02:54, 19 September 2013
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]