Literature DB >> 19609940

Genetic considerations in the prenatal diagnosis of overgrowth syndromes.

Neeta Vora1, Diana W Bianchi.   

Abstract

Large (>90%) for gestational age (LGA) fetuses are usually identified incidentally. Detection of the LGA fetus should first prompt the provider to rule out incorrect dates and maternal diabetes. Once this is done, consideration should be given to certain overgrowth syndromes, especially if anomalies are present. The overgrowth syndromes have significant clinical and molecular overlap, and are associated with developmental delay, tumors, and other anomalies. Although genetic causes of overgrowth are considered postnatally, they are infrequently diagnosed prenatally. Here, we review prenatal sonographic findings in fetal overgrowth syndromes, including Pallister-Killian, Beckwith-Wiedemann, Sotos, Perlman, and Simpson-Golabi-Behmel. We also discuss prenatal diagnosis options and recurrence risks.

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Year:  2009        PMID: 19609940      PMCID: PMC4426974          DOI: 10.1002/pd.2319

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  56 in total

Review 1.  Wiedemann-Beckwith syndrome: further prenatal characterization of the condition.

Authors:  Orit Reish; Israela Lerer; Aliza Amiel; Eli Heyman; Arie Herman; Tzipora Dolfin; Dvorah Abeliovich
Journal:  Am J Med Genet       Date:  2002-01-22

Review 2.  Parental origin of the isochromosome 12p in Pallister-Killian syndrome: molecular analysis of one patient and review of the reported cases.

Authors:  J L Struthers; C D Cuthbert; M M Khalifa
Journal:  Am J Med Genet       Date:  1999-05-21

3.  Perlman syndrome--a cause of enlarged, hyperechogenic kidneys.

Authors:  L S Chitty; T Clark; D Maxwell
Journal:  Prenat Diagn       Date:  1998-11       Impact factor: 3.050

4.  A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly.

Authors:  D D Weaver; C B Graham; I T Thomas; D W Smith
Journal:  J Pediatr       Date:  1974-04       Impact factor: 4.406

5.  A case of nondiabetic macrosomia with Simpson-Golabi-Behmel syndrome: antenatal sonographic findings.

Authors:  H Yamashita; I Yasuhi; T Ishimaru; T Matsumoto; T Yamabe
Journal:  Fetal Diagn Ther       Date:  1995 Mar-Apr       Impact factor: 2.587

6.  Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation.

Authors:  W W Lam; I Hatada; S Ohishi; T Mukai; J A Joyce; T R Cole; D Donnai; W Reik; P N Schofield; E R Maher
Journal:  J Med Genet       Date:  1999-07       Impact factor: 6.318

Review 7.  Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.

Authors:  A Slavotinek; L Gaunt; D Donnai
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

8.  Sonographic findings in Beckwith-Wiedemann syndrome related to H19 hypermethylation.

Authors:  C Le Caignec; C Gicquel; M C Gubler; C Guyot; M C You; A Laurent; M Joubert; N Winer; A David; J M Rival
Journal:  Prenat Diagn       Date:  2004-03       Impact factor: 3.050

9.  A new X-linked mental retardation-overgrowth syndrome.

Authors:  M Golabi; L Rosen
Journal:  Am J Med Genet       Date:  1984-01

10.  Genetics of Sotos syndrome.

Authors:  Remco Visser; Naomichi Matsumoto
Journal:  Curr Opin Pediatr       Date:  2003-12       Impact factor: 2.856

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  7 in total

1.  Two Consecutive Pregnancies with Simpson-Golabi-Behmel Syndrome Type 1: Case Report and Review of Published Prenatal Cases.

Authors:  Konstantin Ridnõi; Elvira Kurvinen; Sander Pajusalu; Tiia Reimand; Katrin Õunap
Journal:  Mol Syndromol       Date:  2018-06-08

Review 2.  Epimutation in inherited metabolic disorders: the influence of aberrant transcription in adjacent genes.

Authors:  Jean-Louis Guéant; Youssef Siblini; Céline Chéry; Guillaume Schmitt; Rosa-Maria Guéant-Rodriguez; David Coelho; David Watkins; David S Rosenblatt; Abderrahim Oussalah
Journal:  Hum Genet       Date:  2022-02-21       Impact factor: 5.881

Review 3.  Modeling human epigenetic disorders in mice: Beckwith-Wiedemann syndrome and Silver-Russell syndrome.

Authors:  Suhee Chang; Marisa S Bartolomei
Journal:  Dis Model Mech       Date:  2020-05-26       Impact factor: 5.758

4.  Co-occurrence of a maternally inherited DNMT3A duplication and a paternally inherited pathogenic variant in EZH2 in a child with growth retardation and severe short stature: atypical Weaver syndrome or evidence of a DNMT3A dosage effect?

Authors:  Katarzyna Polonis; Patrick R Blackburn; Raul A Urrutia; Gwen A Lomberk; Teresa Kruisselbrink; Margot A Cousin; Nicole J Boczek; Nicole L Hoppman; Dusica Babovic-Vuksanovic; Eric W Klee; Pavel N Pichurin
Journal:  Cold Spring Harb Mol Case Stud       Date:  2018-08-01

5.  Fatal adult-onset diaphragmatic hernia in the context of the COVID-19 pandemic.

Authors:  Ajith Antony; Sheryl Suares; André Victor Fernandes
Journal:  Autops Case Rep       Date:  2022-01-14

Review 6.  Regimens of fetal surveillance of suspected large-for-gestational-age fetuses for improving health outcomes.

Authors:  Katherine A T Culliney; Graham K Parry; Julie Brown; Caroline A Crowther
Journal:  Cochrane Database Syst Rev       Date:  2016-04-05

Review 7.  Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review.

Authors:  Jing Liu; Qin Liu; Shuting Yang; Na Ma; Jialun Pang; Ying Peng; Hui Xi; Zhengjun Jia; Yingchun Luo; Meiping Jiang; Yanling Teng; Wenxian Yu; Zhuo Li; Hua Wang
Journal:  Mol Genet Genomic Med       Date:  2021-07-22       Impact factor: 2.183

  7 in total

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