Literature DB >> 3895927

Prenatal diagnosis of Weyers syndrome (deficient ulnar and fibular rays with bilateral hydronephrosis).

B R Elejalde, M M de Elejalde, C Booth, C Kaye, L Hollison.   

Abstract

A fetus with Weyers oligodactyly was studied after a previous sibling had been born with that condition. Prenatal diagnosis was undertaken using ultrasound to visualize the long bones, which were found to be severely affected by the condition at 19 weeks of gestation. Most notable were the ulnae and fibulae, which were very short; the fetus had bilateral hydronephrosis.

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Year:  1985        PMID: 3895927     DOI: 10.1002/ajmg.1320210305

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


  3 in total

1.  Weyers' ulnar ray/oligodactyly syndrome and the association of midline malformations with ulnar ray defects.

Authors:  P D Turnpenny; J C Dean; P Duffty; J A Reid; P Carter
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

2.  Fetal phenotypic analysis.

Authors:  B Rafael Elejalde; Maria Mercedes de Elejalde
Journal:  Indian J Pediatr       Date:  1986-07       Impact factor: 1.967

3.  Ulnar club-hand and constriction-ring syndrome.

Authors:  T Malpas; N Anderson; S Langley
Journal:  Pediatr Radiol       Date:  1995
  3 in total

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