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Managing challenging pain and irritability in OSTM1 mutation-related infantile malignant osteopetrosis
Osteopetrosis describes a heterogeneous group of diseases characterised by increased bone density due to impaired osteoclast. The malignant infantile autosomal recessive (MIOP) form caused by mutations in OSTM1 is the most severe form of osteopetrosis. Children with this phenotype exhibit multisyste...
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| Publicat a: | BMJ Case Rep |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Publishing Group
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8137230/ https://ncbi.nlm.nih.gov/pubmed/34011644 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2021-242498 |
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