Severe cervical dysplasia and nasal cartilage calcification following prenatal warfarin exposure

被引:0
作者
Howe, AM
Lipson, AH
deSilva, M
Ouvrier, R
Webster, WS
机构
[1] UNIV SYDNEY,DEPT ANAT & HISTOL,SYDNEY,NSW 2006,AUSTRALIA
[2] CHILDRENS HOSP,DEPT GENET,SYDNEY,NSW,AUSTRALIA
[3] CHILDRENS HOSP,DEPT RADIOL,SYDNEY,NSW,AUSTRALIA
[4] CHILDRENS HOSP,DEPT NEUROL,SYDNEY,NSW,AUSTRALIA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1997年 / 71卷 / 04期
关键词
warfarin embryopathy; ectopic calcification; stippling; vitamin B; deficiency; Binder syndrome; chondrodysplasia punctata;
D O I
10.1002/(SICI)1096-8628(19970905)71:4<391::AID-AJMG4>3.0.CO;2-X
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We present an infant who was exposed to warfarin throughout pregnancy and has warfarin embryopathy. When the child was examined radiologically at 20 months areas of calcification were visible in the septal and alar cartilages of the small external part of the nose. The location of this ectopic calcification is consistent with that seen in an animal model of the warfarin embryopathy. It supports the hypothesis that warfarin interferes with the prenatal growth of the cartilaginous nasal septum by inhibiting the normal formation of a vitamin K-dependent protein that prevents calcification of cartilage. The child also had severe abnormalities of the cervical vertebrae and secondary damage to the spinal cord. Cervical vertebral anomalies are a relatively common finding in the warfarin embryopathy and in the related Binder syndrome. (C) 1997 Wiley-Liss, Inc.
引用
收藏
页码:391 / 396
页数:6
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