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[皮尔逊综合征:一种基于线粒体DNA缺失的多系统疾病]

[Pearson's syndrome: a multi-system disorder based on a mt-DNA deletion].

作者信息

Danse P W, Jakobs C, Rötig A, Munnich A, Veerman A J

机构信息

Afd. Kindergeneeskunde, Vrije Universiteit Amsterdam.

出版信息

Tijdschr Kindergeneeskd. 1991 Dec;59(6):196-202.

PMID:1776144
Abstract

In 1979 Pearson described a syndrome, in which the main symptoms were severe sideroblastic anemia and exocrine pancreas dysfunction. The aetiology was still unknown. A decade later, the Pearson syndrome can be described as a lethal multisystem disorder, in which the bone marrow and exocrine pancreas show major dysfunction, but also other organs (like kidneys, liver, gut and skin) can be affected. These patients also show growth retardation. The study of the mitochondrial DNA allowed identification of a deletion in the mitochondrial DNA. The case of a patient suffering from Pearson's syndrome is reported.

摘要

1979年,皮尔逊描述了一种综合征,其主要症状为严重的铁粒幼细胞贫血和外分泌胰腺功能障碍。病因仍不明。十年后,皮尔逊综合征可被描述为一种致命的多系统疾病,其中骨髓和外分泌胰腺表现出主要功能障碍,但其他器官(如肾脏、肝脏、肠道和皮肤)也可能受到影响。这些患者还表现出生长发育迟缓。对线粒体DNA的研究发现线粒体DNA存在缺失。本文报告了一例患有皮尔逊综合征的患者病例。

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