Novel fetal and maternal sonographic findings in confirmed cases of Beckwith–Wiedemann syndrome

The objective of the study was to examine the prenatal anomalies in fetuses with Beckwith–Wiedemann syndrome (BWS).

[1]  T. Kuwata,et al.  ‘Stained‐glass’ sign for placental mesenchymal dysplasia , 2014, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[2]  M. Vazquez,et al.  Beckwith-Wiedemann Syndrome: Growth Pattern and Tumor Risk according to Molecular Mechanism, and Guidelines for Tumor Surveillance , 2013, Hormone Research in Paediatrics.

[3]  R. Weksberg,et al.  Molecular Findings in Beckwith–Wiedemann Syndrome , 2013, American journal of medical genetics. Part C, Seminars in medical genetics.

[4]  U. Nayeri,et al.  Systematic review of sonographic findings of placental mesenchymal dysplasia and subsequent pregnancy outcome , 2013, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[5]  D. Cha,et al.  Early Detection of Preeclampsia Using Inhibin A and Other Second-Trimester Serum Markers , 2011, Fetal Diagnosis and Therapy.

[6]  R. Weksberg,et al.  Beckwith–Wiedemann syndrome , 2010, European Journal of Human Genetics.

[7]  L. Wilkins-Haug,et al.  Outcome of fetuses with a prenatal ultrasound diagnosis of isolated omphalocele , 2009, Prenatal diagnosis.

[8]  A. Westerveld,et al.  Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells , 2009, European Journal of Human Genetics.

[9]  Meredith Wilson,et al.  The clinical phenotype of mosaicism for genome‐wide paternal uniparental disomy: Two new reports , 2008, American journal of medical genetics. Part A.

[10]  N. Rahman,et al.  Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation , 2007, Journal of Medical Genetics.

[11]  B. Thilaganathan,et al.  Outcome of antenatally diagnosed abdominal wall defects , 2007, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[12]  K. Aagaard-Tillery,et al.  Beckwith-Wiedemann Syndrome Presenting with an Elevated Triple Screen in the Second Trimester of Pregnancy , 2006, Fetal Diagnosis and Therapy.

[13]  D. Prawitt,et al.  Beckwith–Wiedemann syndrome: multiple molecular mechanisms , 2006, Expert Reviews in Molecular Medicine.

[14]  F. Ghezzi,et al.  The thick heterogeneous (jellylike) placenta: a strong predictor of adverse pregnancy outcome , 2004, Prenatal diagnosis.

[15]  L. Dodds,et al.  Unexplained elevated maternal serum alpha-fetoprotein and/or human chorionic gonadotropin and the risk of adverse outcomes. , 2003, American journal of obstetrics and gynecology.

[16]  Andrew P Feinberg,et al.  Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects. , 2002, American journal of human genetics.

[17]  R. Weksberg,et al.  Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutations. , 2001, Genomics.

[18]  J N Martin,et al.  The amniotic fluid index, single deepest pocket, and two-diameter pocket in normal human pregnancy. , 2000, American journal of obstetrics and gynecology.

[19]  C. J. Colby,et al.  Second-trimester serum chorionic gonadotropin concentrations and complications and outcome of pregnancy. , 1999, The New England journal of medicine.

[20]  L. Gaunt,et al.  Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome. , 1997, Journal of medical genetics.

[21]  Y. Fukushima,et al.  New p57KIP2 mutations in Beckwith-Wiedemann syndrome , 1997, Human Genetics.

[22]  E. Maher,et al.  Beckwith-Wiedermann syndrome , 1994 .

[23]  K. Nicolaides,et al.  Fetal biometry at 14–40 weeks' gestation , 1994, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[24]  D. Luthy,et al.  Presented by invitation at the Fifty-ninth Annual Meeting of the Pacific Coast Obstetrical and Gynecological Society, Ojai, California, October 11-18, 1992. , 1993 .

[25]  D. Luthy,et al.  An association between elevated levels of human chorionic gonadotropin in the midtrimester and adverse pregnancy outcome. , 1993, American journal of obstetrics and gynecology.

[26]  I. Macgillivray,et al.  The classification and definition of the hypertensive disorders of pregnancy. , 1988, American journal of obstetrics and gynecology.

[27]  Nan Faion T. Wu,et al.  The Beckwith-Wiedemann Syndrome , 1974, Clinical pediatrics.

[28]  Wiedemann Hr.  [FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SYNDROME"?] , 1964 .

[29]  H. Wiedemann.  [FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SYNDROME"?]. , 1964, Journal de genetique humaine.