Abstract
Osteogenesis imperfecta(OI)is a genetic bone disease characterized by increased bone fragility and recurrent bone fractures. It belongs to orphan diseases of which the diagnosis and treatment are facing challenges. The effective treatments targeting at the underlying causes are still unavailable. Recently, many agents have been demonstrated to increase bone mineral density, improve bone microstructures, and reduce the incidence of fractures. Herein, we review the progress in new drugs for the treatment of OI.
| Original language | English |
|---|---|
| Pages (from-to) | 173-177 |
| Number of pages | 5 |
| Journal | Journal of International Pharmaceutical Research |
| Volume | 44 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 28 Feb 2017 |
| Externally published | Yes |
Keywords
- Orphan drug
- Osteogenesis imperfect
- Rare disease
Fingerprint
Dive into the research topics of 'New drugs for the treatment of osteogenesis imperfecta: Research advances'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver