Exstrophy of the cloaca in a 47,XXX child: Review of genitourinary malformations in triple‐X patients
- 15 March 1993
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 45 (6) , 761-763
- https://doi.org/10.1002/ajmg.1320450619
Abstract
Cloacal exstrophy, unilateral renal agenesis, and Müllerian anomalies occurred in a live‐born 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.Keywords
This publication has 13 references indexed in Scilit:
- Multiple congenital anomalies associated with a 47,XXX chromosome constitutionAmerican Journal of Medical Genetics, 1990
- Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetusAmerican Journal of Medical Genetics, 1989
- 47, XXX: What Is the Prognosis?Pediatrics, 1988
- Exstrophy, Epispadias, and Cloacal and Urogenital Sinus AbnormalitiesPediatric Clinics of North America, 1987
- Familial Nature of Congenital Absence and Severe Dysgenesis of Both KidneysNew England Journal of Medicine, 1984
- Optimal management of cloacal exstrophyJournal of Pediatric Surgery, 1983
- X‐chromosome polysomy in the female: personal experience and review of the literatureClinical Genetics, 1983
- Clinical and cytogenetic studies on a group of females with XXX sex chromosome complementsThe Journal of Pediatrics, 1964
- The Triple-X SyndromeBMJ, 1961
- EVIDENCE FOR THE EXISTENCE OF THE HUMAN "SUPER FEMALE"The Lancet, 1959