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The amount of cobalamin stored and how the enterohepatic circuit and the buffering of general losses work as levels decrease varies greatly between individuals

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Castilla-Cortzar I, Pascual M, Urdaneta E, Pardo J, Puche JE, Vivas B, Daz-Casares A, Garca M, Daz-Snchez M, Varela-Nieto I, Castilla A, Gonzlez-Barn S

This genetic anomaly in MeCbl synthesis leads to the accumulation of homocysteine, a condition termed hyperhomocysteinemia or homocystinuria [94, 100], (Fig