主页 文献库文献详情
PMID: 3287923 已发表 · ppublish 英语

XK aprosencephaly and anencephaly in sibs.

American journal of medical genetics ·第 29 卷 ·第 3 期 ·1988-06-24

Townes P L, Reuter K, Rosquete E E, Magee B D

摘要

Recent studies have suggested a causal and pathogenetic relationship between holoprosencephaly and anencephaly. In support of the proposed relationship we report a sibship that includes anencephalic male twins and a female infant with a severe form of alobar holoprosencephaly, radial aplasia, and oligodactyly. The upper limb and brain malformations are considered to represent aprosencephaly syndrome. The coexistence of anencephaly and aprosencephaly within a sibship suggests that XK aprosencephaly syndrome may be an autosomal recessive disorder.

文献信息
期刊
American journal of medical genetics
期刊简称
Am J Med Genet
ISSN
0148-7299
发表日期
1988-06-24
收录日期
1988-06-24
更新日期
2004-11-17
语言
英语
国家/地区
United States
NLM ID
7708900
分析服务
分析服务

联系地址

山东省济南市章丘区文博路2号

齐鲁师范学院 genelibs生信实验室

山东省济南市高新区舜华路750号

大学科技园北区F座4单元2楼

电话: 0531-88819269

微信公众号

关注微信订阅号,实时查看信息,关注医学生物学动态。


商务邮箱

E-mail: product@genelibs.com