Abetalipoproteinemia |
Bassen-Kornzweig Syndrome |
Abetalipoproteinemia is a rare genetic disorder that interferes with the normal absorption of fat and fat soluble vitamins from food. Features This disorder leads to a multiple vitamin deficiency, affecting the fat soluble vitamin A, vitamin D, vitamin E, and vitamin K. However, many of the observed effects are due to vitamin E deficiency in particular. Diagnosis The inability to absorb fat in the ileum will result in steatorrhea, or fat in the stool. As a result, this can be clinical ...
Wikipedia - [full article]
Resources
- Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsoma (Google Health)
- Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia (Google Health)
- Bassen-Kornzweig syndrome (Google Health)
- Microsomal triglyceride transfer protein, the abetalipoproteinemia gene product, mediates the se (Google Health)

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