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[从基因到疾病;从呼吸链缺陷基因SDHD到副神经节瘤和嗜铬细胞瘤]

[From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas].

作者信息

Taschner P E M, Bröcker-Vriends A H J T, van der Mey A G L

机构信息

Leids Universitair Medisch Centrum, Postbus 9503, 2300 RA Leiden, Centrum voor Humane en Klinische Genetica.

出版信息

Ned Tijdschr Geneeskd. 2002 Nov 16;146(46):2188-90.

Abstract

Hereditary paragangliomas are rare benign tumours arising from neuroectodermal tissue in the head and neck region. In families with paraganglioma, occasionally adrenal and extra-adrenal pheochromocytomas are found. Paragangliomas, adrenal and extra-adrenal pheochromocytomas may be caused by mutations in the SDHB, SDHC and SDHD genes encoding different subunits of mitochondrial respiratory chain complex II. Most paraganglioma cases in the Netherlands are caused by SDHD mutations. Presymptomatic DNA diagnosis is available for families with paragangliomas caused by SDHD mutations.

摘要

遗传性副神经节瘤是起源于头颈部神经外胚层组织的罕见良性肿瘤。在患有副神经节瘤的家族中,偶尔会发现肾上腺和肾上腺外嗜铬细胞瘤。副神经节瘤、肾上腺和肾上腺外嗜铬细胞瘤可能由编码线粒体呼吸链复合物II不同亚基的SDHB、SDHC和SDHD基因突变引起。荷兰的大多数副神经节瘤病例是由SDHD基因突变引起的。对于由SDHD基因突变导致的副神经节瘤家族,可进行症状前DNA诊断。

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