Literature DB >> 2764022

Dominant inheritance of Wiedemann-Beckwith syndrome: further evidence for transmission of "unstable premutation" through carrier women.

K A Aleck1, T A Hadro.   

Abstract

We report on a 4-generation family in which the Wiedemann Beckwith syndrome (WBS) was transmitted as an autosomal dominant trait. The condition occurred in sibs born to carrier women and in children born to affected mothers. Presumptive carrier women were examined for microsigns of WBS in an attempt to determine whether extreme variability of the disorder, rather than an unaffected carrier state, was present. No minor stigmata of the WBS could be found in the presumptive carriers. Our study supports a previous hypothesis that in some families the WBS can be transmitted in a 2-step process involving first an unstable premutation and then a "telomutation." Because only females appear to be transmitters of the telomutation, an ovum-mediated sex-associated factor may be involved in the process of telomutation.

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Year:  1989        PMID: 2764022     DOI: 10.1002/ajmg.1320330202

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  7 in total

Review 1.  Genomic imprinting: review and relevance to human diseases.

Authors:  J G Hall
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

2.  Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.

Authors:  C Moutou; C Junien; I Henry; C Bonaïti-Pellié
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

3.  Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome.

Authors:  D Viljoen; R Ramesar
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

4.  Uniparental disomy occurs infrequently in Wilms tumor patients.

Authors:  P Grundy; B Wilson; P Telzerow; W Zhou; M C Paterson
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

5.  Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5).

Authors:  N Tommerup; C A Brandt; S Pedersen; L Bolund; J Kamper
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

6.  Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumour.

Authors:  R G Grundy; J Pritchard; M Baraitser; A Risdon; M Robards
Journal:  Eur J Pediatr       Date:  1992-12       Impact factor: 3.183

7.  Insulin-like growth factor 2 cannot be linked to a familial form of Beckwith-Wiedemann syndrome.

Authors:  A Nyström; F Hedborg; R Ohlsson
Journal:  Eur J Pediatr       Date:  1994-08       Impact factor: 3.183

  7 in total

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