A family with Xq22.3q25 interstitial deletion and normal ovarian function

Long Ching Kuan, Mei Tsz Su, Chin Ming Wu, Ming Chen, Pao Lin Kuo, Tsung Cheng Kuo

研究成果: Article同行評審

摘要

Objective: To investigate genomic changes in a family with deletion of X chromosome q22.3-q25 associated with normal constitutional and reproductive phenotypes. Design: Case report. Setting: Academic district hospital genetic laboratory. Patient(s): A family incidentally found to have deletion of X chromosome q22.3-q25. Intervention(s): Cytogenetic analysis and array-based comparative genomic hybridization for amniotic fluid and peripheral blood lymphocyte of family members. Main Outcome Measure(s): Ovarian function and menstrual cycles. Result(s): The proband and two daughters showed deletion of Xq22.3q25. This region spans 17.4 Mb and contains 121 genes. Conclusion(s): Female subjects with deletion of Xq22.3q25 may present with normal constitutional and reproductive phenotypes.

原文English
頁(從 - 到)e29-e34
期刊Fertility and Sterility
96
發行號1
DOIs
出版狀態Published - 2011 7月

All Science Journal Classification (ASJC) codes

  • 生殖醫學
  • 婦產科

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