Literature DB >> 3950488

The congenital warfarin syndrome.

M S Zakzouk.   

Abstract

A rare congenital nasal deformity due to warfarin embryopathy is reported. The commonest anomalies described in this syndrome are: hypoplasia of the nose, stippling of bone, optic atrophy and mental retardation. The various abnormalities and the mechanism of warfarin teratogenesis are discussed.

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Year:  1986        PMID： 3950488     DOI： 10.1017/s0022215100099011

Source DB:  PubMed          Journal:  J Laryngol Otol        ISSN： 0022-2151            Impact factor:   1.469


  4 in total

1.  Identification of two novel transmembrane gamma-carboxyglutamic acid proteins expressed broadly in fetal and adult tissues.

Authors:  J D Kulman; J E Harris; L Xie; E W Davie
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-13       Impact factor: 11.205

Review 2.  Thrombophilia and its treatment in pregnancy.

Authors:  A Eldor
Journal:  J Thromb Thrombolysis       Date:  2001-09       Impact factor: 2.300

3.  Nasal septal and craniofacial form in European- and African-derived populations.

Authors:  Nathan E Holton; Todd R Yokley; Aaron Figueroa
Journal:  J Anat       Date:  2012-07-03       Impact factor: 2.610

4.  Nose: Applied Aspects in Dermatology.

Authors:  Dammaningala Venkataramaiah Lakshmi; Kanathur Shilpa; Holavanahally Veerabhadrappa Nataraja; Kallapa Gorur Divya
Journal:  Indian J Dermatol       Date:  2016 Mar-Apr       Impact factor: 1.494
  4 in total

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