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完全性颅脑脊柱裂和并腿畸形。

Craniorachischisis totalis and sirenomelia.

作者信息

Rodríguez J I, Palacios J

机构信息

Department of Pathology, La Paz Hospital, Madrid, Spain.

出版信息

Am J Med Genet. 1992 Jul 1;43(4):732-6. doi: 10.1002/ajmg.1320430416.

Abstract

We report on a male infant with craniorachischisis totalis and sirenomelia, an association that seems to have been observed only 5 times before. In addition to these anomalies, the patient had hypoplasia of the phalanges of the right thumb. The pattern of associated malformations in infants with anencephaly and sirenomelia is reviewed. This condition, which combines cephalic and caudal defects of the embryo, could be considered an example of the "axial mesodermal dysplasia spectrum" and may be related to the midline developmental field concept.

摘要

我们报告了一名患有完全性颅脑脊柱裂和并腿畸形的男婴,这种关联此前似乎仅被观察到5次。除了这些异常外,该患者右拇指指骨发育不全。对无脑儿和并腿畸形婴儿相关畸形的模式进行了综述。这种合并胚胎头端和尾端缺陷的情况可被视为“轴旁中胚层发育异常谱系”的一个例子,可能与中线发育场概念有关。

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