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) |
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Pages (from-to) | 892-897 |
Number of pages | 6 |
Journal | Pediatric Radiology |
Volume | 38 |
Issue number | 8 |
DOIs | |
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