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Article

Genetic analysis, ultrasound phenotype, and pregnancy outcomes of fetuses with Xp22.33 or Yp11.32 microdeletions.

Journal of perinatal medicine - 29 Jan 2024

Cai Meiying, Chen Xuemei, Li Ying, Lin Na, Huang Hailong, Xu Liangpu

Abstract excerpt

OBJECTIVES: The phenotypes of Xp22.33 or Yp11.32 microdeletions comprising the short-stature homeobox (SHOX) gene have been extensively described in adults and children. Herein, the prenatal ultrasound phenotype and pregnancy outcomes of fetuses with Xp22.33/Yp11.32 microdeletions were analyzed to improve our understanding, diagnosis, and monitoring of this genetic condition in the fetal stage. METHODS: A total...

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PMID: 37846158
DOI: 10.1515/jpm-2023-0190

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