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The Generational Pattern of Biotinidase Deficiency
A deficiency in biotin recycling should theoretically lead to generationally compounded biotinidase deficiency. This is true even though the inheritance is autosomal recessive, which predicts no sex differences and an inheritance pattern typical of blue eyes. The use of the word recessive here is an extremely misleading artifact of the reality distortion imposed on the issue by the medical diagnostic model. If I had children with a woman who did not have a such a deficiency, I would interrupt the inheritance of the depleted biotin pool since my personal biotin status would have nothing to do with the biotin pool left to my children at birth. In reality, carriers have happed the biotinid enzyme activity as non-