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Osteopetrosis and Its Relevance for the Discovery of New Functions Associated with the Skeleton
Osteopetrosis is a rare genetic disorder characterized by an increase of bone mass due to defective osteoclast function. Patients typically displayed spontaneous fractures, anemia, and in the most severe forms hepatosplenomegaly and compression of cranial facial nerves leading to deafness and blindn...
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| Publicado no: | Int J Endocrinol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi Publishing Corporation
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4385565/ https://ncbi.nlm.nih.gov/pubmed/25873953 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/372156 |
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