Journal of Genetic Medicine

  • 제18권2호
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  • Pages.101-104
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  • 2021
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  • 1226-1769(pISSN)
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  • 2383-8442(eISSN)
대한의학유전학회 (Korean Society of Medical Genetics and Genomics)
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A female patient with Xp21 gene deletion syndrome

  • Kim, Jungeun (Department of Pediatrics, Gangnam Severance Children's Hospital, Yonsei University College of Medicine) ;
  • Lee, Hyunjoo (Department of Pediatrics, Gangnam Severance Children's Hospital, Yonsei University College of Medicine) ;
  • Na, Ji-Hoon (Department of Pediatrics, Gangnam Severance Children's Hospital, Yonsei University College of Medicine) ;
  • Lee, Young-Mock (Department of Pediatrics, Gangnam Severance Children's Hospital, Yonsei University College of Medicine)
  • 투고 : 2021.08.05
  • 심사 : 2021.09.03
  • 발행 : 2021.12.31
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초록

Xp21 contiguous gene deletion syndrome is associated with complex glycerol kinase deficiency, congenital adrenal hypoplasia, Duchene muscular dystrophy, and intellectual disability. Xp21 gene deletion syndrome is X-linked recessive, so most symptomatic patients are male, and only a few female symptomatic patients have been reported. We report the first female Korean case of an Xp21 deletion. NGS data were analyzed for copy number variation, and the Xp21 deletion (chr X: 29301056-31838200) was confirmed using real-time PCR.

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참고문헌

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