About Autosomal dominant primary hypomagnesemia with hypocalciuria
Autosomal dominant primary hypomagnesemia with hypocalciuria is a rare disease catalogued by Orphanet (ORPHA:34528). It is associated with the FXYD2 gene. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.
Clinical Trial Eligibility Tips
What to know before applying to Autosomal dominant primary hypomagnesemia with hypocalciuria trials.
Search ClinicalTrials.gov for "Autosomal dominant primary hypomagnesemia with hypocalciuria" or filter by Orphanet code ORPHA:34528 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting Autosomal dominant primary hypomagnesemia with hypocalciuria trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Autosomal dominant primary hypomagnesemia with hypocalciuria. Updated daily.