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先天性脊椎骨骺发育不良。1例组织学检查结果(作者译)

[Congenital spondylo-epiphysial dysplasia. A case with histological findings (author's transl)].

作者信息

Haarmeyer A

出版信息

Z Orthop Ihre Grenzgeb. 1979 Oct;117(5):844-8.

PMID:121497
Abstract

We have reported on an infant suffering from congenital spondylo-epiphysial dysplasia, in whom the autosomally dominant affliction could already be perceived in the baby's age by the relevant affection of the spine and of the proximal epiphyses. Firstly, it should be tried to stop the progredient kyphoscoliosis by a circular brace. A significantly increased mucopolysaccharide separation could biochemically not be stated in 24 h-urine. Gasser cells could not be found in the lymphocytes as proved by Spranger and Wiedmann in five of six patients. The histological investigation of the biopsy material, taken from the posterior iliac crest, resulted in a desmale ossification process which is atypical for this region.

摘要

我们曾报道过一名患有先天性脊椎骨骺发育不良的婴儿,在该婴儿身上,通过脊柱和近端骨骺的相关病变,在其婴儿期就已能察觉到常染色体显性遗传病的影响。首先,应尝试通过环形支架来阻止进行性脊柱后凸侧弯。在24小时尿液中,生化检测未发现黏多糖分离显著增加。如施普朗格和维德曼在6例患者中的5例所证实的那样,淋巴细胞中未发现加塞尔细胞。对取自髂嵴后部的活检材料进行组织学检查,结果显示为该区域非典型的骨化过程。

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