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Biotinidase Deficiency Profound biotinidase deficiency is an autosomal recessive disorder that is characterized by pathogenic variants in the BTD gene that result in enzyme activity that is less than 10% of the normal
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Finally, the medications ability to decrease food noise is a benefit but, in rare cases, can cause severely reduced nutrition intake that prompts ketosis
This may leave some people with only written instructions for drawing up doses and injecting themselves with the drug
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