Osteopetrosis; a report of two Iranian patients with autosomal recessive inheritance pattern

In the rare hereditary bone disorder of osteopetrosis, reduced bone resorption function leads to both the development of densely sclerotic fragile bones and progressive obliteration of the marrow spaces and cranial foramina. Marrow obliteration, typically associated with extramedullary hemopoiesis a...

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Detalles Bibliográficos
Autores principales: Morovvati, Saeid, Amirpour Amraii, Sara, Zahed Shekar Abi, Hosna, Shahbazi, Nastaran, Ranjbar, Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Babol University of Medical Sciences 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920503/
https://www.ncbi.nlm.nih.gov/pubmed/24551774

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920503/
https://www.ncbi.nlm.nih.gov/pubmed/24551774

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