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Update of Diagnostic Evaluation of Craniosynostosis with a Focus on Pediatric Systematic Evaluation and Genetic Studies

  • Hwang, Su-Kyeong (Department of Pediatrics, Kyungpook National University Hospital) ;
  • Park, Ki-Su (Department of Neurosurgery, Kyungpook National University Hospital) ;
  • Park, Seong-Hyun (Department of Neurosurgery, Kyungpook National University Hospital) ;
  • Hwang, Sung Kyoo (Department of Neurosurgery, Kyungpook National University Hospital)
  • 투고 : 2016.01.22
  • 심사 : 2016.02.13
  • 발행 : 2016.05.01

초록

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.

키워드

참고문헌

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피인용 문헌

  1. Serum nickel is associated with craniosynostosis risk: Evidence from humans and mice vol.146, pp.None, 2021, https://doi.org/10.1016/j.envint.2020.106289
  2. Craniosynostosis: Neonatal Perspectives vol.22, pp.4, 2021, https://doi.org/10.1542/neo.22-4-e250