Suppr超能文献

变异性卟啉病:一个大家族的研究(作者译)

[Porphyria variegata: a study of a large family (author's transl)].

作者信息

Husquinet H, Noirfalise A, Parent M T

出版信息

J Genet Hum. 1978 Dec;26(4):367-83.

PMID:752067
Abstract

Porphyria variegata (or South-African porphyria) is not a rare disease in Europe. Its transmission, in a Walloon family, is described. The pedigree extends over 7 generations and comprises 184 individuals. It was possible to carry out biological studies on 100 family members. The results of the analyses are presented and discussed. The levels of fecal porphyrines, the presence of cutaneous lesions and the genealogical relationships permitted the establishment of a coherent picture. Three other families suffering from the same disease are briefly reported. A systematic search for carriers of the gene is indispensable in porphyrias. All identified carriers must be warned of the risks they run and must be supplied with a list of medicaments to be avoided. The prevention of cutaneous lesions by beta-carotene is envisaged.

摘要

混合型卟啉病(或南非卟啉病)在欧洲并非罕见疾病。本文描述了它在一个瓦隆家族中的遗传情况。该家系延续了7代,包含184人。对100名家族成员进行了生物学研究。文中呈现并讨论了分析结果。粪便卟啉水平、皮肤病变的存在情况以及系谱关系使得构建出了一幅连贯的图景。简要报告了另外三个患同一疾病的家族。在卟啉病中,系统筛查基因携带者是必不可少的。必须告知所有已确认的携带者他们所面临的风险,并提供一份应避免使用的药物清单。还设想了用β-胡萝卜素预防皮肤病变。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验