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CHARGE syndrome with early fetal ear abnormalities: A case report.

Yu LiangSi-Jie HeLiuqiao YangTao LiLijian ZhaoCong-Xin Sun
Published in: Clinical case reports (2024)
gene (c.406C > T, p.Q136X in exon 2) was identified to cause the disorder. Our study demonstrated that prenatal diagnosis and genetic testing were recommended to obtain a solid diagnosis of CHARGE syndrome when fetal external ear abnormality was detected by ultrasound examination.
Keyphrases
  • case report
  • magnetic resonance imaging
  • genome wide
  • copy number
  • gene expression
  • computed tomography
  • dna methylation
  • genome wide identification
  • electron transfer