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沃尔夫-赫希霍恩综合征。II. 病理解剖学

The Wolf-Hirschhorn syndrome. II. Pathologic anatomy.

作者信息

Lazjuk G I, Lurie I W, Ostrowskaja T I, Kirillova I A, Nedzved M K, Cherstvoy E D, Silyaeva N F

出版信息

Clin Genet. 1980 Jul;18(1):6-12. doi: 10.1111/j.1399-0004.1980.tb01357.x.

Abstract

Most cases of Wolf-Hirschhorn syndrome occurring among children who die during the perinatal period are not diagnosed by morphologists. However, analysis of the morphological data on the Wolf-Hirschhorn syndrome revels that association of typical external features and abnormalities ofthe brain (shortening of the H2 area of Ammon's horn, dystonic dysplastic gyrae in the cerebellum), eyes (colobomata, microphthalmos, retinal dysplasia) and kidneys (bilateral or unilateral agenesis, cystic dysplasia or polycystosis) with diaphragmatic hernia allows the establishment of a diagnosis of the syndrome without cytogenetic investigation.

摘要

大多数在围产期死亡的儿童中出现的沃尔夫-赫希霍恩综合征病例未被形态学家诊断出来。然而,对沃尔夫-赫希霍恩综合征形态学数据的分析表明,典型的外部特征与大脑(海马角H2区缩短、小脑张力障碍性发育异常脑回)、眼睛(脉络膜缺损、小眼症、视网膜发育异常)和肾脏(双侧或单侧肾缺如、囊性发育异常或多囊症)的异常以及膈疝相关联,这使得在没有细胞遗传学检查的情况下也能确诊该综合征。

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