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

✍ Scribed by Lin, Henry J. ;Ndiforchu, Fombe ;Patell, Shibani


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
428 KB
Volume
45
Category
Article
ISSN
0148-7299

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✦ Synopsis


Cloaca1 exstrophy, unilateral renal agenesis, and Mullerian 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.