Literature DB >> 12704750

Obstetric aspects of the Prader-Willi syndrome.

B F Fong1, J I P De Vries.   

Abstract

The Prader-Willi syndrome (PWS) is a complex, multisystem disorder. The syndrome affects the central nervous system, with a predilection for the hypothalamus. The clinical picture in PWS is very variable, and depends on the age of the affected child. Frequently, the most prominent features such as obesity, mental retardation and behavioral disorders do not become evident until the later childhood stage, which can lead to underdiagnosis or late diagnosis in early childhood. Because of the long-term implications of this syndrome, it is important to recognize its features as soon as possible so that early counseling of parents and the affected child is possible. Because PWS can also lead to complications in both pregnancy and labor, proper diagnosis in the fetus can also help optimize perinatal care in affected children. In three cases we illustrate that certain combinations of obstetric symptoms such as polyhydramnios, diminished fetal movements, malpresentation and abnormal fetal heart rhythm can help alert clinicians to the possibility of this syndrome in fetuses. Copyright 2003 ISUOG. Published by John Wiley & Sons, Ltd.

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Year:  2003        PMID: 12704750     DOI: 10.1002/uog.90

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


  9 in total

Review 1.  Oxytocin as feeding inhibitor: maintaining homeostasis in consummatory behavior.

Authors:  Pawel K Olszewski; Anica Klockars; Helgi B Schiöth; Allen S Levine
Journal:  Pharmacol Biochem Behav       Date:  2010-06-02       Impact factor: 3.533

2.  Comparison of perinatal factors in deletion versus uniparental disomy in Prader-Willi syndrome.

Authors:  June-Anne Gold; Ranim Mahmoud; Suzanne B Cassidy; Virginia Kimonis
Journal:  Am J Med Genet A       Date:  2018-05       Impact factor: 2.802

Review 3.  Benefits and limitations of prenatal screening for Prader-Willi syndrome.

Authors:  Merlin G Butler
Journal:  Prenat Diagn       Date:  2016-10-12       Impact factor: 3.050

4.  Truncating Mutations of MAGEL2, a Gene within the Prader-Willi Locus, Are Responsible for Severe Arthrogryposis.

Authors:  Dan Mejlachowicz; Flora Nolent; Jérome Maluenda; Hanitra Ranjatoelina-Randrianaivo; Fabienne Giuliano; Ivo Gut; Damien Sternberg; Annie Laquerrière; Judith Melki
Journal:  Am J Hum Genet       Date:  2015-09-10       Impact factor: 11.025

5.  Multicentre study of maternal and neonatal outcomes in individuals with Prader-Willi syndrome.

Authors:  Preeti Singh; Ranim Mahmoud; June-Anne Gold; Jennifer L Miller; Elizabeth Roof; Roy Tamura; Elisabeth Dykens; Merlin G Butler; Dan J Driscoll; Virginia Kimonis
Journal:  J Med Genet       Date:  2018-05-18       Impact factor: 6.318

6.  Polyhydramnios and abnormal foetal heart rate patterns in a foetus with Prader-Willi syndrome: A case report.

Authors:  Tsuyoshi Murata; Toma Fukuda; Aya Kanno; Hyo Kyozuka; Akiko Yamaguchi; Hiromi Shimizu; Takafumi Watanabe; Keiya Fujimori
Journal:  Case Rep Womens Health       Date:  2020-05-29

7.  Schaaf-Yang syndrome overview: Report of 78 individuals.

Authors:  John McCarthy; Philip J Lupo; Erin Kovar; Megan Rech; Bret Bostwick; Daryl Scott; Katerina Kraft; Tony Roscioli; Joel Charrow; Samantha A Schrier Vergano; Edward Lose; Robert Smiegel; Yves Lacassie; Christian P Schaaf
Journal:  Am J Med Genet A       Date:  2018-10-10       Impact factor: 2.802

8.  Perinatal features of Prader-Willi syndrome: a Chinese cohort of 134 patients.

Authors:  Lili Yang; Qiong Zhou; Bo Ma; Shujiong Mao; Yanli Dai; Mingqiang Zhu; Chaochun Zou
Journal:  Orphanet J Rare Dis       Date:  2020-01-21       Impact factor: 4.123

9.  Evaluation of chromosomal abnormalities and copy number variations in late trimester pregnancy using cordocentesis.

Authors:  Meiying Cai; Na Lin; Yuan Lin; Hailong Huang; Liangpu Xu
Journal:  Aging (Albany NY)       Date:  2020-08-15       Impact factor: 5.682

  9 in total

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