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Angeborene sklerosierende und hyperostotische Skelettveränderungen

  • Chapter
Skeletterkrankungen

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Zusammenfassung

In der Pariser Nomenklatur werden sklerosierende Skelettdysplasien unter dem Subtitel „Abnormalities of density of cortical diaphyseal structure or metaphyseal modelling or both“ zusammengefaßt (Maroteaux 1970). Nach der 1977 überarbeiteten Version gehören folgende Krankheitsbilder dazu:

  • Osteopetrose mit früher Manifestation

  • Osteopetrose mit verzögerter Manifestation

  • Pyknodysostose

  • Osteopoikilie

  • Osteopathia striata

  • Melorheostose

  • diaphysäre Dysplasie (Camurati-Engelmann)

  • kraniodiaphysäre Dysplasie

  • endostale Hyperostose

  • autosomal-dominant, Typ Worth

  • autosomal-rezessiv, Typ van Buchem

  • tubuläre Sklerose (Kenny-Caffey)

  • Pachydermoperiostose

  • Osteodysplastie (Melnick-Needles)

  • frontometaphysäre Dysplasie

  • kraniometaphysäre Dysplasie

  • metaphysäre Dysplasie (Pyle)

  • Sklerosteose

  • Dysosteosklerose

  • Osteoektasie mit Hyperphosphatasie (familiäre Hyperphosphatasämie, juveniler M. Paget1)

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Authors and Affiliations

  1. Radiologische Klinik, Zentralkrankenhaus St. Jürgen-Straße, 28205, Bremen, Deutschland

    Prof. Dr. med. Jürgen Freyschmidt

Authors
  1. Prof. Dr. med. Jürgen Freyschmidt
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© 1993 Springer-Verlag Berlin Heidelberg

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Freyschmidt, J. (1993). Angeborene sklerosierende und hyperostotische Skelettveränderungen. In: Skeletterkrankungen. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-09918-6_4

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  • DOI: https://doi.org/10.1007/978-3-662-09918-6_4

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-09919-3

  • Online ISBN: 978-3-662-09918-6

  • eBook Packages: Springer Book Archive

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