24-hydroxylase Deficiency Clinical Trial
Official title:
24-Hydroxylase Deficiency and CYP24A1 Mutation Patient Registry
You are being asked to take part in this research registry because you or your family member is suspected to have a 24-hydroxylase deficiency.
In this registry we propose to establish and maintain a registry of suspected and confirmed patients with 24 hydroxylase deficiency in an effort to collect data for further investigation. This would be the first and only known registry of its kind. These resources would be made widely available to clinicians and research scientists within Mayo to stimulate advances in the diagnosis and treatment of patients with this disease. ;