Literature DB >> 11309167

The association of aneuploidy and mild fetal pyelectasis in an unselected population: the results of a multicenter study.

P M Chudleigh1, L S Chitty, M Pembrey, S Campbell.   

Abstract

INTRODUCTION: Mild pyelectasis is a common finding and there is some debate as to its association with aneuploidy. The results of a large, prospective, multicenter study of mild pyelectasis designed to determine the incidence and association with aneuploidy in an unselected population are reported.
METHODS: A large multicenter, prospective observational study of unselected fetuses with mild pyelectasis identified between 16 and 26 weeks' gestation in routine ultrasound departments.
RESULTS: There were 737 fetuses with mild pyelectasis of which 12 had an abnormal karyotype. Pyelectasis was isolated in three fetuses with Down syndrome, but in one the mother was older (36 years).
CONCLUSION: These data confirm the fact that the presence of mild fetal pyelectasis increases the risk for aneuploidy, in particular trisomy 21. However, other risk factors should be considered before embarking on fetal karyotyping, as for most pregnancies complicated by isolated mild pyelectasis, risks of aneuploidy will remain small.

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Year:  2001        PMID: 11309167     DOI: 10.1046/j.1469-0705.2001.00360.x

Source DB:  PubMed          Journal:  Ultrasound Obstet Gynecol        ISSN: 0960-7692            Impact factor:   7.299


  7 in total

1.  Prenatal Aneuploidies Computerized Screening (SCA TEST): a pilot study on 1000 women.

Authors:  Alessandro Sacco; Claudio Coco; Lucia Mangiafico; Pietro Cignini; Alessandra Tiezzi; Claudio Giorlandino
Journal:  J Prenat Med       Date:  2007-10

Review 2.  Ultrasonographic soft markers of aneuploidy in second trimester: are we lost?

Authors:  Sameer Raniga; P D Desai; Hetal Parikh
Journal:  MedGenMed       Date:  2006-01-11

Review 3.  Fetal hydronephrosis: is there hope for consensus?

Authors:  Sanna Toiviainen-Salo; Laurent Garel; Andrée Grignon; Josee Dubois; Françoise Rypens; Jacques Boisvert; Gilles Perreault; Jean Claude Decarie; Denis Filiatrault; Chantale Lapierre; Marie-Claude Miron; Nancy Bechard
Journal:  Pediatr Radiol       Date:  2004-04-24

4.  A novel mutation in the renal V2 receptor gene in a boy with trisomy 21.

Authors:  Yasuko Fujisawa; Takeshi Miyamoto; Kyo Furuhashi; Shinichiro Sano; Yuichi Nakagawa; Takehiko Ohzeki
Journal:  Pediatr Nephrol       Date:  2004-03-30       Impact factor: 3.714

Review 5.  Prenatal diagnosis of congenital renal and urinary tract malformations.

Authors:  A Hindryckx; L De Catte
Journal:  Facts Views Vis Obgyn       Date:  2011

6.  Prevalence of defined ultrasound findings of unknown significance at the second trimester fetal anomaly scan and their association with adverse pregnancy outcomes: the Welsh study of mothers and babies population-based cohort.

Authors:  Lisa Hurt; Melissa Wright; Frank Dunstan; Susan Thomas; Fiona Brook; Susan Morris; David Tucker; Marilyn Ann Wills; Colin Davies; Gareth John; David Fone; Shantini Paranjothy
Journal:  Prenat Diagn       Date:  2015-11-20       Impact factor: 3.050

7.  The Welsh study of mothers and babies: protocol for a population-based cohort study to investigate the clinical significance of defined ultrasound findings of uncertain significance.

Authors:  Lisa Hurt; Melissa Wright; Fiona Brook; Susan Thomas; Frank Dunstan; David Fone; Gareth John; Sue Morris; David Tucker; Marilyn Ann Wills; Lyn Chitty; Colin Davies; Shantini Paranjothy
Journal:  BMC Pregnancy Childbirth       Date:  2014-05-08       Impact factor: 3.007

  7 in total

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