Update of Diagnostic Evaluation of Craniosynostosis with a Focus on Pediatric Systematic Evaluation and Genetic Studies
Journal of Korean Neurosurgical Society
;
: 214-218, 2016.
Article
in English
| WPRIM
| ID: wpr-42455
ABSTRACT
Most craniosynostoses are sporadic, but may have an underlying genetic basis. Secondary and syndromic craniosynostosis accompanies various systemic diseases or associated anomalies. Early detection of an associated disease may facilitate the interdisciplinary management of patients and improve outcomes. For that reason, systematic evaluation of craniosynostosis is mandatory. The authors reviewed systematic evaluation of craniosynostosis with an emphasis on genetic analysis.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Craniosynostoses
/
Diagnosis
Type of study:
Diagnostic study
/
Screening study
Limits:
Humans
Language:
English
Journal:
Journal of Korean Neurosurgical Society
Year:
2016
Type:
Article
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