Sandbox: malabsorption: Difference between revisions
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* Low [[Vitamin A|vitamins A]], [[Vitamin D|D]], E, and K | * Low [[Vitamin A|vitamins A]], [[Vitamin D|D]], E, and K | ||
* [[Anemia]] | * [[Anemia]] | ||
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* [[Genetic defects]] in ''SLC10A2'' (solute carrier family 10 member 2 gene) | * [[Genetic defects]] in ''SLC10A2'' (solute carrier family 10 member 2 gene) | ||
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* Total and specific [[bile | * Total and specific [[bile acids]] from stool | ||
* | * Gamma emitter selenium-75-homocholic acid taurine ([[SeHCAT]]) | ||
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! align="center" style="background:#DCDCDC;" |[[Abetalipoproteinemia]] | ! align="center" style="background:#DCDCDC;" |[[Abetalipoproteinemia]] | ||
| align="center" style="background:#F5F5F5;" | | | style="padding: 5px 5px; background: #F5F5F5;" align="center" |Infancy | ||
| align="center" | | Adult | ||
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* [[Abdominal distension | | style="padding: 5px 5px; background: #F5F5F5;" align="left" | | ||
* | * [[Abdominal distension]] | ||
* [[Visual field defect]] | |||
* [[Dysarthria]] | * [[Dysarthria]] | ||
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* Low [[triglyceride]] | * Low [[triglyceride]] | ||
* Low total [[cholesterol]] levels | * Low total [[cholesterol]] levels | ||
* [[Acanthocytes]] | * [[Acanthocytes]] | ||
* Low [[vitamin E]] levels | * Low [[vitamin E]] levels | ||
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* | * Visual impairment | ||
* [[Ataxia]] | * [[Ataxia]] | ||
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* [[Autosomal recessive]] disorder caused by mutations encoding the [[microsomal]] [[triglyceride]] transfer protein (MTP) | * [[Autosomal recessive]] disorder caused by mutations encoding the [[microsomal]] [[triglyceride]] transfer protein (MTP) | ||
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* Clinical findings and low [[triglyceride]] and [[cholesterol]] level | * Clinical findings and low [[triglyceride]] and [[cholesterol]] level | ||
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! align="center" style="background:#DCDCDC;" |[[Microscopic colitis]] | ! align="center" style="background:#DCDCDC;" |[[Microscopic colitis]] |
Revision as of 21:50, 9 November 2017
Abbreviations: WBC: White blood cells; Plt: Platelets, Hgb: Hemoglobin, IgE: Immunoglobulin E, IgA: Immunoglobulin A
Cause | Peak age of onset | History | Physical exam | Lab findings | Additional findings | Cause/Pathogenesis | Gold standard diagnosis | ||||||||
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Fever | Abdominal pain | Diarrhea | Weight loss | ||||||||||||
Watery | Fatty | WBC | Hgb | Plt | Other lab findings | ||||||||||
Whipple's disease | 40-60 | +/- | + | + | + | + |
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↓ | ↓ | ↓/↑ |
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Celiac disease | Childhood
Adult |
- | + | +/- | +/- | + | - | ↓ | - |
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Cystic fibrosis | Childhood
Adult |
+ | + | - | + | + |
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Crohns disease | Young adults
(20th) |
+ | + | + | + | + | ↑ | ↓ |
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Irritable bowel syndrome | 30-50 | - | +/- | +/- | +/- | - |
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- | - | - |
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VIPoma | 30-50 | - | + | + | + | + |
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Zollinger-Ellison syndrome) | 20-50 |
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Lactose intolerance | Any age | + |
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Eosinophilic gastroenteritis | 30th | - | + | + | + | + | ↑ | - | - |
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Primary bile acid malabsorption | Childhood Adult | ↓ |
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Abetalipoproteinemia | Infancy
Adult |
- | - | - |
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Microscopic colitis | 60th | + | - | + | + |
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Hyperthyroidism | Any age | + | - | + | +/- |
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Grain allergy | Childhood | - | + | + | - | + |
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