MATTHEW-WOOD SYNDROME: A CASE WITH DEXTROCARDIA AND STREAK GONADS

被引:0
|
作者
Cubuk, P. Ozyavuz [1 ]
Ho, L. [2 ]
Reversade, B. [2 ,3 ]
Percin, E. F. [1 ]
机构
[1] Gazi Univ, Fac Med, Dept Med Genet, TR-06500 Ankara, Turkey
[2] ASTAR, Inst Med Biol, Human Embryol Lab, Singapore, Singapore
[3] Natl Univ Singapore, Dept Paediat, Singapore, Singapore
来源
GENETIC COUNSELING | 2016年 / 27卷 / 03期
关键词
Matthew Wood syndrome; STRA6; gene; Anophthalmia; Dextrocardia; Streak gonads; STRA6; MUTATIONS; VITAMIN-A; ANOPHTHALMIA; MALFORMATIONS; SPECTRUM;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Matthew-Wood syndrome: a case with dextrocardia and streak gonads: Matthew-Wood syndrome (MWS), also termed Microphthalmia, syndrome 9 (MCOPS9, MIM 601186), Spear syndrome, or pulmonary hypoplasia, diaphragmatic hernia, anophthalmia and cardiac defects syndrome (PDAC syndrome), is an autosomal recessive disorder characterised by ocular, respiratory and cardiac abnormalities. Mutations in retinoic acid 6 gene (STRA6) have been reported in clinically diagnosed patients with MWS. Here we presented a case with MWS, who has characteristic findings of the syndrome as well as dextrocardia as an undescribed feature, and bilateral streak gonads which was described only in one patient previously. Molecular analysis showed a homozygous exonic missense mutation in the STRA6 gene.
引用
收藏
页码:405 / 410
页数:6
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