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

Lin, Henry J. ; Ndiforchu, Fombe ; Patell, Shibani

American journal of medical genetics, 1993-03, Vol.45 (6), p.761-763

New York: Wiley Subscription Services, Inc., A Wiley Company

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Título:
Exstrophy of the cloaca in a 47,XXX child: Review of genitourinary malformations in triple-X patients
Autor: Lin, Henry J. ; Ndiforchu, Fombe ; Patell, Shibani
Assuntos: Abnormalities, Multiple - genetics ; Anus, Imperforate - genetics ; Biological and medical sciences ; Chromosome aberrations ; cloaca ; Cloaca - abnormalities ; exstrophy ; Female ; genitourinary malformations ; Hernia, Umbilical - genetics ; Humans ; Infant ; Kidney - abnormalities ; Medical genetics ; Medical sciences ; Ovary - abnormalities ; triple-X ; Trisomy ; Urogenital Abnormalities ; Uterus - abnormalities ; X Chromosome
É parte de: American journal of medical genetics, 1993-03, Vol.45 (6), p.761-763
Notas: ArticleID:AJMG1320450619
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SourceType-Scholarly Journals-1
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ObjectType-Review-1
ObjectType-Feature-5
ObjectType-Report-2
ObjectType-Article-4
Descrição: 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. © 1993 Wiley‐Liss, Inc.
Editor: New York: Wiley Subscription Services, Inc., A Wiley Company
Idioma: Inglês

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