Literature DB >> 6674415

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

A Nivelon-Chevallier, A Mavel, R Michiels, M Bethenod.   

Abstract

A new family with Wiedeman-Beckwith Syndrome is reported. All the affected subjects are conceived from normal sisters. In two cases, antenatal diagnosis has been established by ultrasound examination which showed an exomphalos. In one case, pathological examination of the abortus product confirmed the diagnosis.

Entities:  

Mesh:

Year:  1983        PMID: 6674415

Source DB:  PubMed          Journal:  J Genet Hum        ISSN: 0021-7743


  2 in total

1.  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

2.  The incidence of cardiac lesions in infants born with major gastrointestinal malformations in Northern Ireland.

Authors:  A J Thompson; H C Mulholland
Journal:  Ulster Med J       Date:  2000-05
  2 in total

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