Literature DB >> 1245966

Warfarin therapy initiated during pregnancy and phenotypic chondrodysplasia punctata.

R M Pauli, J D Madden, K J Kranzler, W Culpepper, R Port.   

Abstract

An infant is described who has clinical manifestations and roentgenographic features consistent with the diagnosis of chondrodysplasia punctata. The mother of this infant received warfarin during pregnancy. Eight cases demonstrating an association between warfarin therapy during pregnancy and chondrodysplasia punctata in the child have been reported; in the present case therapy was initiated following conception (see following case report). Warfarin may be teratogenic, producing a phencopy of the heritable forms of chondrodysplasia punctata. Because of the evident association we suggest (1) warfarin is contraindicated in pregnancy and alternative anticoagulants should be used; (2) products of at-risk pregnancies should be screened for the characteristic radiologic findings; and (3) preconceptual counselling and antenatal diagnosis of the disease may be beneficial.

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Year:  1976        PMID: 1245966     DOI: 10.1016/s0022-3476(76)80281-8

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  5 in total

1.  Fetal environment and congenital malformations.

Authors:  D N Singh
Journal:  Indian J Pediatr       Date:  1989 Sep-Oct       Impact factor: 1.967

2.  Chondrodysplasia punctata and maternal warfarin treatment.

Authors:  A Abbott; J R Sibert; J B Weaver
Journal:  Br Med J       Date:  1977-06-25

3.  Chondrodysplasia punctata after warfarin in early pregnancy. Case report and summary of the literature.

Authors:  M F Whitfield
Journal:  Arch Dis Child       Date:  1980-02       Impact factor: 3.791

4.  Association of congenital deficiency of multiple vitamin K-dependent coagulation factors and the phenotype of the warfarin embryopathy: clues to the mechanism of teratogenicity of coumarin derivatives.

Authors:  R M Pauli; J B Lian; D F Mosher; J W Suttie
Journal:  Am J Hum Genet       Date:  1987-10       Impact factor: 11.025

5.  The congenital warfarin syndrome: a case report.

Authors:  M Baillie; E D Allen; A R Elkington
Journal:  Br J Ophthalmol       Date:  1980-08       Impact factor: 4.638

  5 in total

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