Case report of a 22-week fetus with 47,XXX karyotype and multiple lower mesodermal defects

Mai P. Hoang; Kathleen S. Wilson; Nancy R. Schneider; Charles F. Timmons

doi:10.1007/s100249900090

Case report of a 22-week fetus with 47,XXX karyotype and multiple lower mesodermal defects

Mai P. Hoang, Kathleen S. Wilson, Nancy R. Schneider, Charles F. Timmons

Research output: Contribution to journal › Article › peer-review

21 Scopus citations

Abstract

A 22-week stillborn fetus with 47,XXX karyotype had lower mesodermal defects consisting of irregular fusion of the sacral vertebrae, anal agenesis, multicystic dysplasia of a horseshoe kidney, a single umbilical artery, dysplastic ovaries, and uterine hypoplasia. This case provides additional evidence for an association between trisomy X and genitourinary defects including lower mesodermal defects sequence.

Original language	English (US)
Pages (from-to)	58-61
Number of pages	4
Journal	Pediatric and Developmental Pathology
Volume	2
Issue number	1
DOIs	https://doi.org/10.1007/s100249900090
State	Published - Jan 1999

Keywords

Genitourinary malformations
Lower mesodermal defects
Triple-X

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Pathology and Forensic Medicine

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10.1007/s100249900090

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abstract = "A 22-week stillborn fetus with 47,XXX karyotype had lower mesodermal defects consisting of irregular fusion of the sacral vertebrae, anal agenesis, multicystic dysplasia of a horseshoe kidney, a single umbilical artery, dysplastic ovaries, and uterine hypoplasia. This case provides additional evidence for an association between trisomy X and genitourinary defects including lower mesodermal defects sequence.",

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Case report of a 22-week fetus with 47,XXX karyotype and multiple lower mesodermal defects

Abstract

Keywords

ASJC Scopus subject areas

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