Literature DB >> 1583639

Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome.

D Viljoen1, R Ramesar.   

Abstract

A previously unreported family in which seven members in two generations have Beckwith-Wiedemann syndrome (BWS) is documented. Paternal imprinting of the gene responsible for BWS is involved as the mechanism responsible for the aberrant inheritance pattern in this kindred. A review of published reports showed 27 previously published pedigrees with two or more affected subjects with BWS. Paternal imprinting would explain the non-mendelian inheritance of BWS in all but four kindreds. The latter families are examined in more detail and in only one example is the evidence against imprinting totally unexplained.

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Year:  1992        PMID: 1583639      PMCID: PMC1015916          DOI: 10.1136/jmg.29.4.221

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  29 in total

1.  Beckwith-Wiedemann syndrome in a mother and her son.

Authors:  E Ben-Galim; E Gross-Kieselstein; A Abrahamov
Journal:  Am J Dis Child       Date:  1977-07

2.  E.M.G. syndrome.

Authors:  H R Wiedemann
Journal:  Lancet       Date:  1973-09-15       Impact factor: 79.321

3.  Wiedemann-Beckwith syndrome.

Authors:  R M Forrester
Journal:  Lancet       Date:  1973-07-07       Impact factor: 79.321

4.  [Wiedemann and Beckwith syndrome: a new familial case].

Authors:  C Piussan; B Risbourg; C Lenaerts; N Delvallez; M F Gontier; M Vitse
Journal:  J Genet Hum       Date:  1980-09

5.  Letter: Wiedemann-Beckwith syndrome.

Authors:  N Matsuura; M Endo; T Okayasu; A Okuno
Journal:  Lancet       Date:  1975-09-13       Impact factor: 79.321

6.  Familial occurrence of the Wiedemann-Beckwith syndrome and persistent fontanel.

Authors:  A Sommer; E A Cutler; B L Cohen; D Harper; C Backes
Journal:  Am J Med Genet       Date:  1977

7.  Familial macroglossia-omphalocele syndrome.

Authors:  J Chemke
Journal:  J Genet Hum       Date:  1976-12

8.  Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases.

Authors:  A L Kosseff; J Herrmann; E F Gilbert; C Viseskul; M Lubinsky; J M Opitz
Journal:  Eur J Pediatr       Date:  1976-10-01       Impact factor: 3.183

9.  [Familial Wiedeman-Beckwith syndrome: prenatal echography diagnosis and histologic confirmation].

Authors:  A Nivelon-Chevallier; A Mavel; R Michiels; M Bethenod
Journal:  J Genet Hum       Date:  1983-12

10.  Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome.

Authors:  M Waziri; S R Patil; J W Hanson; J A Bartley
Journal:  J Pediatr       Date:  1983-06       Impact factor: 4.406

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  16 in total

Review 1.  Genomic imprinting: implications for human disease.

Authors:  J G Falls; D J Pulford; A A Wylie; R L Jirtle
Journal:  Am J Pathol       Date:  1999-03       Impact factor: 4.307

2.  Beckwith-Wiedemann syndrome.

Authors:  A M Norman; A P Read; D Donnai
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

3.  The importance of differentiating Simpson-Golabi-Behmel and Beckwith-Wiedemann syndromes.

Authors:  R Hughes-Benzie; J Allanson; A Hunter; T Cole
Journal:  J Med Genet       Date:  1992-12       Impact factor: 6.318

4.  Nonparametric method for detecting imprinting effect using all members of general pedigrees with missing data.

Authors:  Fangyuan Zhang; Shili Lin
Journal:  J Hum Genet       Date:  2014-08-14       Impact factor: 3.172

Review 5.  Beckwith-Wiedemann syndrome.

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

6.  CDKN1C expression in Beckwith-Wiedemann syndrome patients with allele imbalance.

Authors:  E M Algar; G J Deeble; P J Smith
Journal:  J Med Genet       Date:  1999-07       Impact factor: 6.318

7.  Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.

Authors:  D Catchpoole; W W Lam; D Valler; I K Temple; J A Joyce; W Reik; P N Schofield; E R Maher
Journal:  J Med Genet       Date:  1997-05       Impact factor: 6.318

8.  Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus.

Authors:  A Nordenskjöld; F Hedborg; H Luthman; M Nordenskjöld
Journal:  Hum Genet       Date:  1993-10-01       Impact factor: 4.132

9.  Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia.

Authors:  Birgitt Müller; Katja Hedrich; Norman Kock; Natasa Dragasevic; Marina Svetel; Jennifer Garrels; Olfert Landt; Matthias Nitschke; Peter P Pramstaller; Wolf Reik; Eberhard Schwinger; Jürgen Sperner; Laurie Ozelius; Vladimir Kostic; Christine Klein
Journal:  Am J Hum Genet       Date:  2002-11-20       Impact factor: 11.025

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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