Literature DB >> 3044795

Wiedemann-Beckwith syndrome.

W Engström1, S Lindham, P Schofield.   

Abstract

The Wiedemann-Beckwith syndrome (WBS) comprises an accumulation of multiple congenital anomalies. Exomphalos, macroglossia and gigantism are considered the most common manifestations, hence the alternative designation EMG-syndrome. The syndrome carries with it an increased risk of developing specific tumours. One of the more frequent metabolic changes is transient neonatal hypoglycaemia, the result of increased insulin secretion. Inheritance of the syndrome remains uncertain. Most cases are sporadic, but a number of familial cases have been reported. Present evidence suggests that WBS is an autosomal dominant trait with variable expressivity. This review summarizes the abundant literature on the subject and discusses recent molecular genetic developments that may explain the interrelationship between the clinical abnormalities, metabolic disturbances and development of tumours.

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Year:  1988        PMID: 3044795     DOI: 10.1007/BF00441965

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  87 in total

1.  Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy.

Authors:  C Turleau; J de Grouchy
Journal:  Ann Genet       Date:  1985

2.  Metabolic aspects of the Beckwith-Wiedemann syndrome.

Authors:  D Schiff; E Colle; D Wells; L Stern
Journal:  J Pediatr       Date:  1973-02       Impact factor: 4.406

3.  Insulin-like growth factors (IGF) 1 and 2 in human foetal plasma and relationship to gestational age and foetal size during midpregnancy.

Authors:  I K Ashton; J Zapf; I Einschenk; I Z MacKenzie
Journal:  Acta Endocrinol (Copenh)       Date:  1985-12

4.  Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling.

Authors:  A C Berry; E M Belton; C Chantler
Journal:  J Med Genet       Date:  1980-04       Impact factor: 6.318

5.  The Beckwith-Wiedemann syndrome. The exomphalos-macroglossia-gigantism syndrome.

Authors:  N F Wu; T Kushnick
Journal:  Clin Pediatr (Phila)       Date:  1974-05       Impact factor: 1.168

6.  Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome.

Authors:  R A Spritz; D Mager; R M Pauli; R Laxova
Journal:  Am J Hum Genet       Date:  1986-08       Impact factor: 11.025

7.  The birth prevalence of malformation syndromes in Tokyo infants: a survey of 14,430 newborn infants.

Authors:  M Higurashi; K Iijima; Y Sugimoto; N Ishikawa; H Hoshina; N Watanabe; K Yoneyama
Journal:  Am J Med Genet       Date:  1980

8.  Pancreoblastoma in a neonate associated with Beckwith-Wiedemann syndrome.

Authors:  S R Potts; S Brown; M D O'Hara
Journal:  Z Kinderchir       Date:  1986-02

9.  [Somatomedin activity in Wiedemann-Beckwith syndrome].

Authors:  M Weninger; A Lischka; A Pollak; C Vergesslich; E Ogris; H Frisch
Journal:  Monatsschr Kinderheilkd       Date:  1984-12       Impact factor: 0.323

Review 10.  Insulin-like growth factor (IGF)/somatomedin receptor subtypes: structure, function, and relationships to insulin receptors and IGF carrier proteins.

Authors:  M M Rechler; S P Nissley
Journal:  Horm Res       Date:  1986
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  23 in total

Review 1.  renal tumors and tumor-like lesions in pediatric patients.

Authors:  J M Kissane; L P Dehner
Journal:  Pediatr Nephrol       Date:  1992-07       Impact factor: 3.714

2.  Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11.

Authors:  A Nyström; J E Cheetham; W Engström; P N Schofield
Journal:  Eur J Pediatr       Date:  1992-07       Impact factor: 3.183

Review 3.  Transcriptional regulation and biological significance of the insulin like growth factor II gene.

Authors:  W Engström; A Shokrai; K Otte; M Granérus; A Gessbo; P Bierke; A Madej; M Sjölund; A Ward
Journal:  Cell Prolif       Date:  1998 Oct-Dec       Impact factor: 6.831

Review 4.  Beckwith-Wiedemann syndrome.

Authors:  M Elliott; E R Maher
Journal:  J Med Genet       Date:  1994-07       Impact factor: 6.318

5.  Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes.

Authors:  J Eggenschwiler; T Ludwig; P Fisher; P A Leighton; S M Tilghman; A Efstratiadis
Journal:  Genes Dev       Date:  1997-12-01       Impact factor: 11.361

6.  Maternal Hypomethylation of KvDMR in a Monozygotic Male Twin Pair Discordant for Beckwith-Wiedemann Syndrome.

Authors:  S C Elalaoui; I Garin; A Sefiani; G Perez de Nanclares
Journal:  Mol Syndromol       Date:  2013-11-30

7.  Congenital craniofacial dysostosis and cutis gyratum: the Beare-Stevenson syndrome.

Authors:  B Bratanic; M Praprotnik; M Novosel-Sever
Journal:  Eur J Pediatr       Date:  1994-03       Impact factor: 3.183

8.  Molecular analysis of patients with Wiedemann-Beckwith syndrome. I. Gene dosage on the short arm of chromosome 11.

Authors:  A Nyström; W Engström; J Cheetham; P N Schofield
Journal:  Eur J Pediatr       Date:  1992-07       Impact factor: 3.183

Review 9.  Medullary sponge kidneys and unilateral Wilms tumour in a child with Beckwith-Wiedemann syndrome.

Authors:  R Beetz; O Schofer; H Riedmiller; R Schumacher; P Gutjahr
Journal:  Eur J Pediatr       Date:  1991-05       Impact factor: 3.183

10.  The cell type-specific IGF2 expression during early human development correlates to the pattern of overgrowth and neoplasia in the Beckwith-Wiedemann syndrome.

Authors:  F Hedborg; L Holmgren; B Sandstedt; R Ohlsson
Journal:  Am J Pathol       Date:  1994-10       Impact factor: 4.307

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