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瑞典首例先天性红细胞生成性卟啉病,以及对该病卟啉排泄模式的修正观点。

The first Swedish case of congenital erythropoietic porphyria, with a revised view of the porphyrin excretion pattern in this disease.

作者信息

Stenberg B, With T K

出版信息

Acta Derm Venereol Suppl (Stockh). 1982;100:87-90.

PMID:6962640
Abstract

A case of congenital erythropoietic porphyria (CEP) in a Swedish boy is described. It is the second case of this extremely rare disease encountered in Scandinavia. Like the first Scandinavian case--a Norwegian boy--this patient showed a porphyrin excretion pattern like that of porphyria cutanea tarda (PCT) which was regarded as pointing to a hepatic type of porphyria. In the Norwegian boy this was regarded as atypical, but our study of the literature revealed two older cases with features pointing to a similar pattern and disclosed that analysis of the porphyrin pattern with modern methods, such as thin-layer chromatography, has not been performed in the great majority of the cases of CEP, because such methods were not available at the time these cases were published. Therefore, it is necessary to study more cases of CEP with modern analytical methods in order to get an adequate picture of the porphyrin pattern typical of this disease.

摘要

本文描述了一名瑞典男孩患先天性红细胞生成性卟啉病(CEP)的病例。这是斯堪的纳维亚半岛发现的第二例这种极其罕见的疾病。与第一例斯堪的纳维亚病例——一名挪威男孩一样,该患者的卟啉排泄模式与迟发性皮肤卟啉病(PCT)相似,这被认为表明是肝型卟啉病。在挪威男孩中,这被视为非典型情况,但我们对文献的研究发现了另外两例具有类似模式特征的更早期病例,并发现,由于在这些病例发表时还没有现代方法(如薄层色谱法),绝大多数CEP病例尚未用这些方法对卟啉模式进行分析。因此,有必要用现代分析方法研究更多的CEP病例,以便充分了解这种疾病典型的卟啉模式。

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