Exstrophy of the cloaca in a 47,XXX child: review of genitourinary malformations in triple-X patients.
Lin HJ , Ndiforchu F , Patell S 
Am J Med Genet.1993 Mar 15 ; 45(6):761-3.
PubMedで表示
Google翻訳で開く
Department of Pediatrics, Harbor-UCLA Medical Center, Torrance 90502.
(5,277view , 1users)
Full Text Sources
Medical
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.
PMID: 8456857 [PubMed - indexed for MEDLINE]
PMID: 8456857 [PubMed - indexed for MEDLINE]
関連論文
- Multiple congenital anomalies associated with a 47,XXX chromosome constitution.
- [Review] Complete duplication of the bladder, urethra, vagina, and uterus in girls.
- Exstrophy of the cloaca and exstrophy of the bladder: two different expressions of a primary developmental field defect.
- OEIS complex (omphalocele-exstrophy-imperforate anus-spinal defects): a review of 14 cases.
- OEIS complex associated with chromosome 1p36 deletion: a case report and review.