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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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Detalhes bibliográficos
Main Authors: Morovvati, Saeid, Amirpour Amraii, Sara, Zahed Shekar Abi, Hosna, Shahbazi, Nastaran, Ranjbar, Reza
Formato: Artigo
Idioma:Inglês
Publicado em: Babol University of Medical Sciences 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3920503/
https://ncbi.nlm.nih.gov/pubmed/24551774
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