47,XXY with Associated Bilateral Renal Agenesis.
We describe the case of a 36-week gestational-age male stillborn with bilateral renal agenesis and a 47,XXY karyotype, as well as features of Potter sequence. No other congenital abnormalities were noted. Severe oligohydramnios was diagnosed prenatally at 30 weeks, and cytogenetic analysis was performed postmortem. Urinary tract anomalies are uncommon in association with Klinefelter syndrome. Unilateral renal agenesis has been described. We describe, to our knowledge, the first case of bilateral renal agenesis in association with 47,XXY.
Published In/Presented At
Barroeta, J. E., & Stopyra, G. A. (2004). 47,XXY with associated bilateral renal agenesis. Archives Of Pathology & Laboratory Medicine, 128(3), e44-e45.
Medical Pathology | Pathology
Department of Pathology and Laboratory Medicine, Pathology Laboratory Medicine Faculty, USF-LVHN SELECT Program