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Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities.
Zhou, Yuan-Yuan; Du, Yu-Fang; Lu, Qing; Zhai, Xiu-Zhang; Shi, Ming-Fang; Chen, Dan-Yun; Liu, Sun-Rong; Zhong, Ying.
Afiliação
  • Zhou YY; Department of Clinical Laboratory, The Third Affiliated Hospital of Guangxi Medical University, Nanning, China.
  • Du YF; Department of Clinical Laboratory, The Third Affiliated Hospital of Guangxi Medical University, Nanning, China.
  • Lu Q; Department of Clinical Laboratory, The Third Affiliated Hospital of Guangxi Medical University, Nanning, China.
  • Zhai XZ; Department of Clinical Laboratory, The Third Affiliated Hospital of Guangxi Medical University, Nanning, China.
  • Shi MF; Department of Clinical Laboratory, The Third Affiliated Hospital of Guangxi Medical University, Nanning, China.
  • Chen DY; Department of Clinical Laboratory, The Third Affiliated Hospital of Guangxi Medical University, Nanning, China.
  • Liu SR; Department of Clinical Laboratory, The Third Affiliated Hospital of Guangxi Medical University, Nanning, China.
  • Zhong Y; Department of Clinical Laboratory, The Third Affiliated Hospital of Guangxi Medical University, Nanning, China.
Front Genet ; 13: 853907, 2022.
Article em En | MEDLINE | ID: mdl-35464846
Background: Musculocontractural Ehlers-Danlos syndrome (mcEDS) is a rare heritable connective tissue disease with various symptoms. The diagnosis of mcEDS is difficult because of the large overlap of clinical symptoms between different EDS subtypes. Methods: We performed karyotype analysis, gene copy number variation detection, whole-exome sequencing, and Sanger sequencing to reveal the underlying genetic etiology of a fetus with structural abnormalities in feet and kidneys. Results: A likely pathogenic mutation [NM_130468.3 c.958C>T (p.Arg320*)] and an uncertain significance mutation [NM_130468.3 c.896A>G (p.Tyr299Cys)] were identified in the carbohydrate sulfotransferase 14 (CHST14) gene by whole-exome sequencing and validated by Sanger sequencing. Conclusion: The two identified mutations appear highly likely to be the genetic causes of the fetal structural abnormalities.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China País de publicação: Suíça