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Family Center

The Biotinidase Deficiency Family Support Group created the Family Center as a place for sharing our children, our experiences with Biotinidase Deficiency, and supporting each other in good times and bad. Please check out what we have to offer and weigh in with your experiences. We'd love to hear from you.

If there's something you would like to see added to the family center please contact our webmaster with your ideas.



The information contained in this website should not be used as a substitute for the medical care and advice of your doctor. There may be variations in treatment that your doctor may recommend based on individual facts and circumstances.

If you find problems with this site please contact our webmaster.
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