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3 Ongoing Care, not just refills Your plan includes ongoing physician oversight, dose adjustment, side-effect support, and lab review when needed all in writing, no required calls

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Biotinidase Deficiency Profound biotinidase deficiency is an autosomal recessive disorder that is characterized by mutations in the BTD gene that result in enzyme activity that is less than 10% of the normal

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Without adequate B12, nerve signals cannot transmit properly, potentially leading to neurological complications