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Retrospective Genetic Analysis of 200 Cases of Sudden Infant Death Syndrome and Its Relationship with Long QT Syndrome in Korea.

Min-Jeong SonMin-Kyoung KimKyung-Moo YangByung-Ha ChoiBong Woo LeeSeong Ho Yoo
Published in: Journal of Korean medical science (2018)
This genetic investigation of LQTS in SIDS showed a low diagnostic yield. These findings suggest that LQTS molecular autopsy could be cautiously conducted in selected cases with family involvement to improve the available genetic counseling information. Meanwhile, a national SIDS registry should be established to document and evaluate the genetic risk of SIDS in Korea.
Keyphrases
  • genome wide
  • copy number
  • case report
  • healthcare
  • dna methylation
  • gene expression
  • quality improvement
  • single molecule
  • social media