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Vitamin B12 malabsorption: Mammalian physiology and acquired and inherited disorders

Monday, April 8, 2013 4:56
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Home of Kyle J. Norton for The Better of Living & Living Health Cobalt is one of many essential mineral needed by our body  in very small amounts to enhance productions of red blood cell and the formation of myelin nerve coverings It also is vital as a necessary cofactor for making the thyroid hormone thyroxine and stored in the red blood cells, the plasma,  liver, kidney, spleen, pancreas, etc.
Vitamin B12 malabsorption: Mammalian physiology and acquired and inherited disordersVitamin B12 (cobalamin) is a cobalt-containing compound synthesized by bacteria and an essential nutrient in mammals. According to the study by the Hospitalier National d’Ophtalmologie des Quinze-Vingts, malabsorption of vitamin B12 is most commonly seen in the elderly, selective pediatric, nondietary-induced B12 deficiency is generally due to inherited disorders including the Imerslund-Gräsbeck syndrome and the much rarer intrinsic factor deficiency. Biochemical, clinical and genetic research on these disorders considerably improved our knowledge of vitamin B12 absorption(10).
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Sources
(10) http://www.ncbi.nlm.nih.gov/pubmed/23178706 http://medicaladvisorjournals.blogspot.com



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