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Results 1 - 10 of 44 for vitamin E
  1. Ataxia with vitamin E deficiency 
    Ataxia with vitamin E deficiency is a disorder that impairs the body's ability to use vitamin E obtained from the diet. Vitamin E is an antioxidant, which means ...
    https://medlineplus.gov/.../ataxia-with-vitamin-e-deficiency - Genetics
  2. Familial hypobetalipoproteinemia 
    ... as well as fat-soluble vitamins such as vitamin E and vitamin A. This difficulty in fat absorption leads to ...
    https://medlineplus.gov/.../familial-hypobetalipoproteinemia - Genetics
  3. Abetalipoproteinemia 
    ... a severe shortage (deficiency) of fat-soluble vitamins (vitamins A, E, and K). The signs and symptoms of this ...
    https://medlineplus.gov/genetics/condition/abetalipoproteinemia - Genetics
  4. Congenital bile acid synthesis defect type 1 
    ... absorb fats and fat-soluble vitamins, such as vitamins A, D, E, and K. People with congenital bile acid synthesis defect type 1 cannot produce (synthesize) bile acids, which are a component of ... fats and fat-soluble vitamins. As a result, an abnormal form of bile ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-1 - Genetics
  5. Congenital bile acid synthesis defect type 2 
    ... absorb fats and fat-soluble vitamins, such as vitamins A, D, E, and K. People with congenital bile acid synthesis defect type 2 cannot produce (synthesize) bile acids, which are a component of ... fats and fat-soluble vitamins. As a result, an abnormal form of bile ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-2 - Genetics
  6. Holocarboxylase synthetase deficiency 
    ... Baumgartner MR. Vitamin-responsive disorders: cobalamin, folate, biotin, vitamins B1 and E. Handb Clin Neurol. 2013;113:1799-810. doi: ...
    https://medlineplus.gov/.../holocarboxylase-synthetase-deficiency - Genetics
  7. Progressive familial intrahepatic cholestasis 
    ... pancreatitis), and low levels of fat-soluble vitamins (vitamins A, D, E, and K) in the blood. Affected individuals typically ...
    https://medlineplus.gov/...ressive-familial-intrahepatic-cholestasis - Genetics
  8. Pyridoxine-dependent epilepsy 
    ... Disorders (NORD) ClinicalTrials.gov EPILEPSY, EARLY-ONSET, 4, VITAMIN B6-DEPENDENT; EPEO4 PubMed Bok LA, Struys E, Willemsen MA, Been JV, Jakobs C. Pyridoxine-dependent ...
    https://medlineplus.gov/.../condition/pyridoxine-dependent-epilepsy - Genetics
  9. Idiopathic infantile hypercalcemia 
    ... exposure in patients with impaired 24-hydroxylation of vitamin D due to CYP24A1 mutations. Am J Kidney Dis. 2015 Jan;65(1):122-6. doi: 10.1053/j.ajkd.2014.06.037. Epub 2014 Nov 4. Citation on PubMed Pronicka E, Ciara E, Halat P, Janiec A, Wojcik M, ...
    https://medlineplus.gov/.../idiopathic-infantile-hypercalcemia - Genetics
  10. Vitamin D-dependent rickets 
    ... binding to hormone response elements: a cause of vitamin D resistance. Proc Natl Acad Sci U S A. 2003 May 13;100(10):6109-14. doi: 10.1073/pnas.1031395100. Epub 2003 Apr 25. Citation on PubMed or Free article on PubMed Central Durmaz E, Zou M, Al-Rijjal RA, Bircan I, Akcurin ...
    https://medlineplus.gov/.../condition/vitamin-d-dependent-rickets - Genetics
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