Craniometaphyseal Dysplasia: A Case Report
Journal of the Korean Radiological Society
;
: 905-907, 1997.
Article
in Korean
| WPRIM
| ID: wpr-55687
ABSTRACT
Craniometaphyseal dysplasia is a rare genetic bone disorder characterized by cranial hyperostosis, sclerosis, and failure of normal modeling of the tubular bones. Both autosomal dominant and recessive forms have been described. Diagnosis of the craniometaphyseal dysplasia is mode on the basis of characteristic radiographic findings. Radiologic findings are thickening and hyperostosis of the skull, and Erlenmeyer flask deformity of the metaphysis on the long bones. We report a case of the craniometaphyseal dysplasia.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Sclerosis
/
Skull
/
Congenital Abnormalities
/
Hyperostosis
/
Diagnosis
Type of study:
Diagnostic study
/
Prognostic study
Language:
Korean
Journal:
Journal of the Korean Radiological Society
Year:
1997
Type:
Article
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