Low LDL causes: Difference between revisions

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|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Dermatologic'''
| '''Dermatologic'''
|bgcolor="Beige"| [[Benign symmetrical lipomatosis of Madelung]], [[dyskeratosis congenita]]
|bgcolor="Beige"| [[Dyskeratosis congenita]], [[Lipoma|lipomatosis of Madelung]]  
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Drug Side Effect'''
| '''Drug Side Effect'''
|bgcolor="Beige"| [[Clofibrate]], [[colesevelam hydrochlorie]], [[colestyramine]], [[doxazosin]], [[lipid lowering drugs]], [[nicotinic acid]], [[NSAID's]], [[prazosin]], [[probucol]], [[statins]]
|bgcolor="Beige"| [[Clofibrate]], [[Colesevelam (patient information)|colesevelam hydrochlorie]], [[colestyramine]], [[doxazosin]], [[nicotinic acid]], [[NSAID]], [[prazosin]], [[probucol]], [[statins]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
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|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Gastroenterologic'''
| '''Gastroenterologic'''
|bgcolor="Beige"| [[Celiac disease]], [[chronic liver disease]], [[chronic pancreatitis]], [[cirrhosis]], [[Crohn's disease]], [[exocrine pancreatic insufficiency]], [[intestinal lymphangiectasia]], [[liver failure]], [[portosystemic shunts]], [[protein losing enteropathies]], [[short bowel syndrome]]
|bgcolor="Beige"| [[Celiac disease]], [[chronic liver disease]], [[chronic pancreatitis]], [[cirrhosis]], [[Crohn's disease]], [[exocrine pancreatic insufficiency]], [[Lymphangiectasia|intestinal lymphangiectasia]], [[liver failure]], [[Transjugular intrahepatic portosystemic shunt|portosystemic shunts]], [[protein losing enteropathy]], [[short bowel syndrome]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Genetic'''
| '''Genetic'''
|bgcolor="Beige"| [[Abetalipoproteinemia]], [[apolipoprotein B deficiency]], [[apoprotein E deficiency]], [[Bassen-Kornzweig disease]], [[cystic fibrosis]], [[deficiency of proprotein convertase subtilisin-like/kexin type 9 (pcsk9)]], [[dyskeratosis congenita]], [[familial alphalipoprotein deficiency]], [[familial hypobetalipoproteinemia]], [[hyperlipoproteinemia, familial type 5]], [[hypobetalipoproteinemia]], [[lipoprotein lipase deficiency]], [[mutations of the MTTP gene]], [[Shwachman-Diamond syndrome]]
|bgcolor="Beige"| [[Abetalipoproteinemia]], [[apolipoprotein B deficiency]], [[Abetalipoproteinemia|Bassen-Kornzweig disease]], [[cystic fibrosis]], [[PCSK9#PCSK9 Deficiency|deficiency of proprotein convertase subtilisin-like/kexin type 9]], [[dyskeratosis congenita]], [[familial alphalipoprotein deficiency]], [[familial hypobetalipoproteinemia]], [[Hyperlipoproteinemia|hyperlipoproteinemia, familial type 5]], [[hypobetalipoproteinemia]], [[lipoprotein lipase deficiency]], [[Abetalipoproteinemia|mutations of the MTTP gene]], [[Shwachman-Diamond syndrome]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
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*[[Amyloidosis]]
*[[Amyloidosis]]
*[[Apolipoprotein B deficiency]]
*[[Apolipoprotein B deficiency]]
*[[Apoprotein E deficiency]]
*[[Autoimmune diseases]]
*[[Autoimmune diseases]]
*[[Bassen-Kornzweig disease]]
*[[Abetalipoproteinemia|Bassen-Kornzweig disease]]
*[[Benign symmetrical lipomatosis of Madelung]]
*[[Celiac disease]]
*[[Celiac disease]]
*[[Chronic liver disease]]
*[[Chronic liver disease]]
Line 143: Line 141:
*[[Cirrhosis]]
*[[Cirrhosis]]
*[[Clofibrate]]
*[[Clofibrate]]
*[[Colesevelam hydrochlorie]]
*[[Colesevelam (patient information)|Colesevelam hydrochlorie]]
*[[Colestyramine]]
*[[Colestyramine]]
{{col-break|width=33%}}
*[[Crohn's disease]]
*[[Crohn's disease]]
*[[Cystic fibrosis]]
*[[Cystic fibrosis]]
*[[Deficiency of proprotein convertase subtilisin-like/kexin type 9 (pcsk9)]]
{{col-break|width=33%}}
*[[PCSK9#PCSK9 Deficiency|Deficiency of proprotein convertase subtilisin-like/kexin type 9]]
*[[Doxazosin]]
*[[Doxazosin]]
*[[Dyskeratosis congenita]]
*[[Dyskeratosis congenita]]
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*[[Familial hypobetalipoproteinemia]]
*[[Familial hypobetalipoproteinemia]]
*[[Giardiasis]]
*[[Giardiasis]]
*[[Hyperlipoproteinemia, familial type 5]]
*[[Hyperlipoproteinemia|Hyperlipoproteinemia, familial type 5]]
*[[Hypobetalipoproteinemia]]
*[[Hypobetalipoproteinemia]]
*[[Inflammatory cytokines]]
*[[Inflammatory cytokines]]
*[[Intestinal lymphangiectasia]]
*[[Lymphangiectasia|Intestinal lymphangiectasia]]
*[[Ketogenic diet]]
*[[Ketogenic diet]]
*[[Lipid lowering drugs]]
*[[Lipoma|Lipomatosis of Madelung]]
*[[Lipoprotein lipase deficiency]]
*[[Lipoprotein lipase deficiency]]
*[[Liver failure]]
{{col-break|width=33%}}
{{col-break|width=33%}}
*[[Liver failure]]
*[[Malignancy]]
*[[Malignancy]]
*[[Malnutrition]]
*[[Malnutrition]]
*[[Ménétrier's disease]]
*[[Ménétrier's disease]]
*[[Mutations of the MTTP gene]]
*[[Abetalipoproteinemia|Mutations of the MTTP gene]]
*[[Nicotinic acid]]
*[[Nicotinic acid]]
*[[NSAID's]]
*[[NSAID]]
*[[Portosystemic shunts]]
*[[Transjugular intrahepatic portosystemic shunt|Portosystemic shunts]]
*[[Prazosin]]
*[[Prazosin]]
*[[Probucol]]
*[[Probucol]]
*[[Protein losing enteropathies]]
*[[Protein losing enteropathy]]
*[[Serum amyloid A]]
*[[Serum amyloid A]]
*[[Short bowel syndrome]]
*[[Short bowel syndrome]]

Revision as of 20:31, 6 November 2013

Low Density Lipoprotein Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Rim Halaby, M.D. [3]; Vendhan Ramanujam M.B.B.S [4]

Overview

Causes

Life Threatening Causes

Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.

Common Causes

Causes by Organ System

Cardiovascular No underlying causes
Chemical/Poisoning No underlying causes
Dental No underlying causes
Dermatologic Dyskeratosis congenita, lipomatosis of Madelung
Drug Side Effect Clofibrate, colesevelam hydrochlorie, colestyramine, doxazosin, nicotinic acid, NSAID, prazosin, probucol, statins
Ear Nose Throat No underlying causes
Endocrine No underlying causes
Environmental Ketogenic diet, malnutrition
Gastroenterologic Celiac disease, chronic liver disease, chronic pancreatitis, cirrhosis, Crohn's disease, exocrine pancreatic insufficiency, intestinal lymphangiectasia, liver failure, portosystemic shunts, protein losing enteropathy, short bowel syndrome
Genetic Abetalipoproteinemia, apolipoprotein B deficiency, Bassen-Kornzweig disease, cystic fibrosis, deficiency of proprotein convertase subtilisin-like/kexin type 9, dyskeratosis congenita, familial alphalipoprotein deficiency, familial hypobetalipoproteinemia, hyperlipoproteinemia, familial type 5, hypobetalipoproteinemia, lipoprotein lipase deficiency, mutations of the MTTP gene, Shwachman-Diamond syndrome
Hematologic Acute myeloid leukemia
Iatrogenic Portosystemic shunts, Short bowel syndrome
Infectious Disease Giardiasis
Musculoskeletal/Orthopedic No underlying causes
Neurologic No underlying causes
Nutritional/Metabolic Abetalipoproteinemia, apolipoprotein B deficiency, Bassen-Kornzweig disease, familial alphalipoprotein deficiency, familial hypobetalipoproteinemia, hyperlipoproteinemia, familial type 5, hypobetalipoproteinemia, lipoprotein lipase deficiency, mutations of the MTTP gene
Obstetric/Gynecologic No underlying causes
Oncologic Acute myeloid leukemia, malignancy
Ophthalmologic No underlying causes
Overdose/Toxicity No underlying causes
Psychiatric No underlying causes
Pulmonary No underlying causes
Renal/Electrolyte No underlying causes
Rheumatology/Immunology/Allergy Acute phase proteins, amyloidosis, autoimmune diseases, celiac disease, inflammatory cytokines, serum amyloid A, Sjrogren's syndrome
Sexual No underlying causes
Trauma No underlying causes
Urologic No underlying causes
Miscellaneous No underlying causes

Causes in Alphabetical Order

References


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