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Results 11 - 20 of 45 for vitamin E
  1. Methylmalonic acidemia with homocystinuria 
    ... H, Hohne W, Longo N, Pasquali M, Mengel E, Watkins D, Shoubridge EA, Majewski J, Rosenblatt DS, Fowler B, Rutsch F, Baumgartner MR. Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism. Nat Genet. 2012 Oct;44(10): ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  2. Cerebral folate transport deficiency 
    ... develops from a shortage (deficiency) of the B-vitamin folate (also called vitamin B9) in the brain. Affected children have normal ... where it attaches (binds) to folate, allowing the vitamin to be brought into the cell. Folate receptor ...
    https://medlineplus.gov/.../cerebral-folate-transport-deficiency - Genetics
  3. Chylomicron retention disease 
    ... the normal absorption of fats, cholesterol, and certain vitamins from food. The features of chylomicron retention disease ... nutrients. Chylomicrons are needed to absorb fat-soluble vitamins and carry fats and cholesterol from the small ...
    https://medlineplus.gov/.../condition/chylomicron-retention-disease - Genetics
  4. Hereditary folate malabsorption 
    ... with the body's ability to use certain vitamins from food. During digestion, the body cannot take in (absorb) certain B vitamins called folates. Folates are important for cell growth ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  5. Transcobalamin deficiency 
    ... impairs the transport of cobalamin (also known as vitamin B12) within the body. Cobalamin is obtained from the diet; this vitamin is found in animal products such as meat, ...
    https://medlineplus.gov/genetics/condition/transcobalamin-deficiency - Genetics
  6. Biotinidase deficiency 
    ... which the body is unable to recycle the vitamin biotin. If this condition is not recognized and ... called biotinidase. This enzyme recycles biotin, a B vitamin found in foods such as liver, egg yolks, ...
    https://medlineplus.gov/genetics/condition/biotinidase-deficiency - Genetics
  7. Primary sclerosing cholangitis 
    ... As a result, weight loss and shortages of vitamins that are absorbed with and stored in fats (fat-soluble vitamins) can occur. A fat-soluble vitamin called vitamin ...
    https://medlineplus.gov/.../condition/primary-sclerosing-cholangitis - Genetics
  8. Hartnup disease 
    ... amino acids to produce other substances, such as vitamins and proteins. Most people with Hartnup disease are able to get the vitamins and other substances they need with a well- ...
    https://medlineplus.gov/genetics/condition/hartnup-disease - Genetics
  9. Riboflavin transporter deficiency neuronopathy 
    ... the SLC52A3 gene. Both proteins move (transport) a vitamin called riboflavin (also called vitamin B2) across the cell membrane. Riboflavin cannot be ... for absorbing riboflavin during digestion so that the vitamin can be used in the body. The RFVT2 ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  10. Spina bifida 
    ... a protein that is involved in processing the vitamin folate (also called vitamin B9). A shortage (deficiency) of this vitamin is an established risk factor for neural tube ...
    https://medlineplus.gov/genetics/condition/spina-bifida - Genetics
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