Exstrophy of the cloaca in a 47,XXX child: review of genitourinary malformations in triple-X patients

American Journal of Medical Genetics
H J LinS Patell

Abstract

Cloacal exstrophy, unilateral renal agenesis, and Müllerian anomalies occurred in a liveborn infant with a 47,XXX chromosome constitution. The patient extends the range of genitourinary anomalies reported in triple-X patients. Screening asymptomatic patients for urinary tract abnormalities may be useful in searching for silent malformations potentially associated with this karyotype.

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Citations

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