Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX
β Scribed by H. Ben Hamouda; N. Mkacher; H. Elghezal; H. Bannour; M. Kamoun; H. Soua; A. Saad; M.M. Souissi; M.T. Sfar
- Book ID
- 116648827
- Publisher
- Masson Editeur
- Year
- 2009
- Tongue
- French
- Weight
- 497 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0368-2315
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract **BACKGROUND:** An association between the tripleβX syndrome (47,XXX) and gastrointestinal malformations is extremely rare. Most 47,XXX patients present with a normal phenotype, but genitourinary malformations have been described. **CASE:** We report a case of a child with 47,XXX and du
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 us