Decade-Long watch: tracking a rare Bone-Weakening disease

NCT ID NCT03745521

Summary

This study aims to observe 226 patients with X-linked hypophosphatemia (XLH), a rare genetic bone disorder, for up to 10 years. Researchers will track the disease's natural progression, the physical and emotional burden on patients, and the long-term effects of treatments. The goal is to gather detailed information to better understand and manage this condition.

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Contacts and locations

Locations

  • Osaka University Hospital

    Osaka, Japan

Conditions

Explore the condition pages connected to this study.