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同胞中的无脑畸形和无脑儿

XK aprosencephaly and anencephaly in sibs.

作者信息

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

机构信息

Department of Pediatrics, University of Massachusetts Medical Center, Worcester 01605.

出版信息

Am J Med Genet. 1988 Mar;29(3):523-8. doi: 10.1002/ajmg.1320290308.

Abstract

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.

摘要

近期研究表明全前脑畸形与无脑畸形之间存在因果及发病机制上的关联。为支持这一关联,我们报告了一个家系,其中包括无脑畸形的男性双胞胎以及一名患有严重型无叶全前脑畸形、桡骨发育不全和少指畸形的女婴。上肢和脑部畸形被认为代表前脑发育不全综合征。家系中无脑畸形和前脑发育不全综合征并存提示XK前脑发育不全综合征可能是一种常染色体隐性疾病。

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