[凋亡和组织病理学骨改变]。

Q4 Medicine
Cesko-Slovenska Pediatrie Pub Date : 1993-08-01
V Bzdúch, E Véghová, S Galbavý, G Matejková, G Olejníková
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引用次数: 0

摘要

作者描述了一个新生儿与死亡细胞性贫血的骨组织病理变化。x线表现为ⅰ型,组织病理改变按Langer分类为ⅱ型。父母的血缘关系提示常染色体隐性遗传,作者认为两个一级表兄妹存在伪异位发育不良是偶然的巧合。所描述的病例证实了假定的临床和遗传异质性的死亡细胞增多症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Thanatophoric nanism and histopathologic bone changes].

The authors describe in a neonate with thanatophoric nanism histopathological changes of the bones. According to X-ray findings type I was involved, the histopathological changes corresponded to type II according to Langer's classification. The consanguinity of the parents suggested the autosomal recessive type of heredity and the presence of pseudo-diastrophic dysplasia in two grade 1 cousins is considered by the authors as an incidental coincidence. The described case confirms the assumed clinical and genetic heterogeneity of thanatophoric nanism.

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来源期刊
Cesko-Slovenska Pediatrie
Cesko-Slovenska Pediatrie Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.30
自引率
0.00%
发文量
32
期刊介绍: So stúpajúcou prevalenciou exogénnej obezity v detskom veku je pozorovaný i čoraz častejší výskyt zmien v lipidovom a sacharidovom metabolizme. Ich mediátorom je inzulínová reziste...
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