HOME | PRODUCTS | OSTEOPOROSIS | Otosclerosis| BIOTINIDASE DEFICIENCY | RESEARCH | CONTACT US | PRIVACY POLICY

 

HOW COMMON IS BIOTINIDASE DEFICIENCY?

Biotinidase deficiency is very rare.


Biotinidase deficiency is a rare metabolic disorder. Only about 1 in 60,000 babies is born with profound or partial biotinidase deficiency. Although you may feel very alone having a child with biotinidase deficiency, there are many other families who share your concerns. Worldwide, more than 150 children have been diagnosed with this condition because they developed symptoms, and more than 300 children have been diagnosed by newborn screening.

 

Introduction 
What is Biotinidase Deficiency?
How will Biotinidase Deficiency Affect my Child's Health? 
What is Partial Biotinidase Deficiency? 
How is Biotinidase Deficiency Treated? 
How is Biotinidase Deficiency Detected? 
How Common is Biotinidase Deficiency? 
What Causes Biotinidase Deficiency? 
How is Biotinidase Deficiency Inherited? 
What can I Expect from my Child? 
What New Research is Being Done? 
Where Can We Get Help? 
References 
Points to Remember

 

These statement on mericon-industries.com have not been evaluated by the Food and Drug Administration. The products and research on this website are not intended to diagnose, treat or cure or prevent disease.

 

Mericon Industries, Inc

All Rights Reserved 1998-2010