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Craniofacial and temporal bone CT findings in cleidocranial dysplasia

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Abstract

Cleidocranial dysplasia (CCD) is a multistructural polyostotic genetic disorder that results from mutation of the CBFA1 gene. Hearing loss is a frequent finding in CCD. We describe the CT craniofacial findings in CCD and provide a comprehensive discussion of the CT temporal bone findings in these patients.

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Acknowledgement

We thank Dr. Mark Volk for his support and assistance with this project.

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Author notes

  1. Guido E. Gonzalez

    Present address: Departamento de Imágenes, Clínica Alemana de Santiago, Santiago, Chile

Authors and Affiliations

  1. Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA

    Guido E. Gonzalez & Juan E. Small

  2. Department of Radiology, Massachusetts Eye and Ear Infirmary and Harvard Medical School, 243 Charles St., Boston, MA, 02114, USA

    Paul A. Caruso, Juan E. Small & Hugh D. Curtin

  3. Department of Otology, Massachusetts Eye and Ear Infirmary and Harvard Medical School, Boston, MA, USA

    Robert W. Jyung

  4. Department of Oral and Maxillofacial Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA

    Maria J. Troulis

Authors
  1. Guido E. Gonzalez
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  2. Paul A. Caruso
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  3. Juan E. Small
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  4. Robert W. Jyung
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  5. Maria J. Troulis
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  6. Hugh D. Curtin
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Corresponding author

Correspondence to Paul A. Caruso.

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Gonzalez, G.E., Caruso, P.A., Small, J.E. et al. Craniofacial and temporal bone CT findings in cleidocranial dysplasia. Pediatr Radiol 38, 892–897 (2008). https://doi.org/10.1007/s00247-008-0866-1

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  • DOI: https://doi.org/10.1007/s00247-008-0866-1

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