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Pycnodysostosis with Osteomyelitis of Maxilla: Case Report of Radiological Analysis
Pycnodysostosis is an autosomal recessive, rare genetic osteosclerotic disorder that caused by mutation in gene coding for Cathepsin K. The bones in pycnodysostosis are abnormally dense and brittle because of insufficient reabsorption process. This syndrome has a number of characteristic clinical an...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer - Medknow
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8035836/ https://www.ncbi.nlm.nih.gov/pubmed/33850408 http://dx.doi.org/10.4103/ccd.ccd_382_17 |