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Abstract

Paget’s disease1 is characterized by excessive, uncoordinated, bone turnover resulting in disorganization of bone architecture, manifested most commonly as thickening, increased bone mass and deformity. Although commonly discussed in texts with the metabolic or generalized bone diseases the disease typically affects part or all of one, several or many bones, but never all the bones and usually only one or two. This simple, and frequently ignored fact, is the single most perplexing and frustrating aspect of the disease when consideration is given to the mechanisms underlying its pathogenesis.

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© 1996 Springer-Verlag Berlin Heidelberg

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Freemont, A.J. (1996). The Pathology of Paget’s Disease. In: The Molecular Biology of Paget’s Disease. Medical Intelligence Unit. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-22505-9_1

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  • DOI: https://doi.org/10.1007/978-3-662-22505-9_1

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-22507-3

  • Online ISBN: 978-3-662-22505-9

  • eBook Packages: Springer Book Archive

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