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

doi:10.1002/ajmg.1320210305

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

Research output: Contribution to journal › Article › peer-review

14 Scopus citations

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.

Original language	English (US)
Pages (from-to)	439-444
Number of pages	6
Journal	American Journal of Medical Genetics
Volume	21
Issue number	3
DOIs	https://doi.org/10.1002/ajmg.1320210305
State	Published - 1985
Externally published	Yes

ASJC Scopus subject areas

Genetics(clinical)

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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.",

author = "Elejalde, {B. R.} and {de Elejalde}, {M. M.} and C. Booth and C. Kaye and L. Hollison",

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AU - Elejalde, B. R.

AU - de Elejalde, M. M.

AU - Booth, C.

AU - Kaye, C.

AU - Hollison, L.

PY - 1985

Y1 - 1985

N2 - 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.

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

Abstract

ASJC Scopus subject areas

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