Exstrophy of the cloaca in a 47,XXX child: review of genitourinary malformations in triple-X patients.
Lin HJ , Ndiforchu F , Patell S
American journal of medical genetics
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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