Your browser doesn't support javascript.
loading
An azoospermic male with a novel chromosome 46, XX, der(15)t(Y; 15)(p11.3; p12).
Wu, Jiebin; Hu, Guanli; Zhai, Jingfang; Han, Conghui; Li, Zhenbei.
Afiliação
  • Wu J; Department of Prenatal Diagnosis Medical Center Xuzhou Central Hospital, Xuzhou Clinical Schools of Nanjing Medical University and Xuzhou Medical University Xuzhou Jiangsu China.
  • Hu G; Department of Prenatal Diagnosis Medical Center Xuzhou Central Hospital, Xuzhou Clinical Schools of Nanjing Medical University and Xuzhou Medical University Xuzhou Jiangsu China.
  • Zhai J; Department of Prenatal Diagnosis Medical Center Xuzhou Central Hospital, Xuzhou Clinical Schools of Nanjing Medical University and Xuzhou Medical University Xuzhou Jiangsu China.
  • Han C; Department of Urology Xuzhou Central Hospital, Xuzhou Clinical Schools of Nanjing Medical University and Xuzhou Medical University Xuzhou Jiangsu China.
  • Li Z; Department of Urology Xuzhou Central Hospital, Xuzhou Clinical Schools of Nanjing Medical University and Xuzhou Medical University Xuzhou Jiangsu China.
Clin Case Rep ; 10(7): e5984, 2022 Jul.
Article em En | MEDLINE | ID: mdl-35846903
Male individuals with a 46, XX karyotype are commonly diagnosed with 46, XX male sex reversal syndrome, one of the rarest sex chromosomal anomalies. In this case, we report a rare XX male with Y-specific DNA sequences located near the end of chromosome 15 p-arm, which was verified by fluorescent in situ hybridization (FISH) as well as copy number variation sequencing (CNV-seq) based on the next- generation sequencing method (>100 Kb). To the best of our knowledge, there have been no reports of XX male with the Yp region transferred to the terminal of chromosome 15 short arm.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2022 Tipo de documento: Article