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This case series examines the prenatal presentation of Klinefelter syndrome (47, XXY), a genetic condition that affects males. The study analyzed prenatal records from 41 cases with a confirmed cytogenetic diagnosis of 47, XXY, and found that increased nuchal translucency was present in 23.1% of cases. In addition, a second-trimester anatomical ultrasound identified Fetal abnormalities in 29.2% of cases. The study highlights the importance of prenatal identification of this condition for accurate counseling and focused prenatal management on ameliorating known complications.
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