Craniofacial and temporal bone CT findings in cleidocranial dysplasia

Guido E. Gonzalez; Paul A. Caruso; Juan E. Small; Robert W. Jyung; Maria J. Troulis; Hugh D. Curtin

doi:10.1007/s00247-008-0866-1

Craniofacial and temporal bone CT findings in cleidocranial dysplasia

Guido E. Gonzalez
, Paul A. Caruso
, Juan E. Small
, Robert W. Jyung
, Maria J. Troulis
, Hugh D. Curtin

Research output: Contribution to journal › Article › peer-review

13 Scopus citations

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.

Original language	English (US)
Pages (from-to)	892-897
Number of pages	6
Journal	Pediatric Radiology
Volume	38
Issue number	8
DOIs	https://doi.org/10.1007/s00247-008-0866-1
State	Published - Aug 2008
Externally published	Yes

All Science Journal Classification (ASJC) codes

Pediatrics, Perinatology, and Child Health
Radiology Nuclear Medicine and imaging

Keywords

Child
Cleidocranial dysplasia

Access to Document

10.1007/s00247-008-0866-1

Cite this

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title = "Craniofacial and temporal bone CT findings in cleidocranial dysplasia",

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.",

keywords = "Child, Cleidocranial dysplasia",

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AU - Gonzalez, Guido E.

AU - Caruso, Paul A.

AU - Small, Juan E.

AU - Jyung, Robert W.

AU - Troulis, Maria J.

AU - Curtin, Hugh D.

PY - 2008/8

Y1 - 2008/8

N2 - 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.

AB - 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.

KW - Child

KW - Cleidocranial dysplasia

UR - https://www.scopus.com/pages/publications/47249144706

UR - https://www.scopus.com/pages/publications/47249144706#tab=citedBy

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M3 - Article

C2 - 18446333

AN - SCOPUS:47249144706

SN - 0301-0449

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JO - Pediatric Radiology

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IS - 8

ER -

Craniofacial and temporal bone CT findings in cleidocranial dysplasia

Abstract

All Science Journal Classification (ASJC) codes

Keywords

Access to Document

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