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Teriparatide in the treatment of recurrent fractures in a Rett patient
Rett syndrome is a common X-linked neurodevelopmental disorder caused by mutations in the MECP2 gene. Patients with Rett syndrome have a low bone mineral density and increased risk of fracture. The present case report describes a successful novel therapeutic intervention with teriparatide with one p...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Clin Cases Miner Bone Metab |
|---|---|
| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
CIC Edizioni Internazionali
2015
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4708971/ https://ncbi.nlm.nih.gov/pubmed/26811706 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11138/ccmbm/2015.12.3.253 |
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