• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

VI型黏多糖贮积症:一种主要与ARSB基因p.R152W突变纯合性相关的心脏表型。

Mucopolysaccharidosis type VI: a predominantly cardiac phenotype associated with homozygosity for p.R152W mutation in the ARSB gene.

作者信息

Jurecka Agnieszka, Zakharova Ekaterina, Cimbalistiene Loreta, Gusina Nina, Kulpanovich Anna, Golda Adam, Opoka-Winiarska Violetta, Piotrowska Ewa, Voskoboeva Elena, Tylki-Szymańska Anna

机构信息

Department of Molecular Biology, University of Gdańsk, Gdańsk, Poland.

出版信息

Am J Med Genet A. 2013 Jun;161A(6):1291-9. doi: 10.1002/ajmg.a.35905. Epub 2013 Apr 30.

DOI:10.1002/ajmg.a.35905
PMID:23633437
Abstract

Mucopolysaccharidosis type VI (MPS VI) is a rare lysosomal, autosomal recessive storage disorder caused by deficient activity of N-acetylgalactosamine-4-sulfatase (ARSB). Approximately, 140 ARSB gene mutations have been identified; however, most are private mutations making genotype-phenotype correlation for most MPS VI patients difficult. The aim of this study was to describe the natural clinical course in patients homozygous for the p.R152W mutation from eight unrelated families. From our database of 70 patients with MPS VI, we selected 10 patients homozygous for the p.R152W mutant allele (median age 27.5 years, range 18-38 years). We performed a cross-sectional observational study characterizing the onset and prevalence of clinical manifestations. First signs of the disease, such as cardiac valve disease, slightly decreased joint range of motion and mild growth retardation, were observed in mid-adolescent years (median 15 years). Within the disease course, the most common clinical feature in all the patients was progressive heart disease of predominantly valve origin leading to symptoms of heart failure. Other typical MPS VI features were subtle and not present in all the patients. Delays up to 23 years (median 8.5 years) intervened between symptom onset and disease diagnosis. Patients homozygous for the p.R152W mutation present a cardiac variant of MPS VI characterized by progressive cardiac valve disease leading to serious cardiac complications including abrupt death due to cardiac failure.

摘要

VI型黏多糖贮积症(MPS VI)是一种罕见的溶酶体常染色体隐性贮积病,由N - 乙酰半乳糖胺 - 4 - 硫酸酯酶(ARSB)活性缺乏引起。大约已鉴定出140种ARSB基因突变;然而,大多数是个别突变,这使得大多数MPS VI患者的基因型 - 表型相关性难以确定。本研究的目的是描述来自8个无关家族的p.R152W突变纯合子患者的自然临床病程。从我们70例MPS VI患者的数据库中,我们选择了10例p.R152W突变等位基因纯合子患者(中位年龄27.5岁,范围18 - 38岁)。我们进行了一项横断面观察性研究,以确定临床表现的起病情况和患病率。在青春期中期(中位年龄15岁)观察到疾病的首发症状,如心脏瓣膜病、关节活动范围略有减小和轻度生长发育迟缓。在疾病过程中,所有患者最常见的临床特征是主要起源于瓣膜的进行性心脏病,导致心力衰竭症状。其他典型的MPS VI特征不明显,并非所有患者都有。症状出现与疾病诊断之间的间隔长达23年(中位8.5年)。p.R152W突变纯合子患者表现出MPS VI的心脏变异型,其特征为进行性心脏瓣膜病,导致严重的心脏并发症,包括因心力衰竭突然死亡。

相似文献

1
Mucopolysaccharidosis type VI: a predominantly cardiac phenotype associated with homozygosity for p.R152W mutation in the ARSB gene.VI型黏多糖贮积症:一种主要与ARSB基因p.R152W突变纯合性相关的心脏表型。
Am J Med Genet A. 2013 Jun;161A(6):1291-9. doi: 10.1002/ajmg.a.35905. Epub 2013 Apr 30.
2
Mucopolysaccharidosis type VI: case report with first neonatal presentation with ascites fetalis and rapidly progressive cardiac manifestation.黏多糖贮积症 VI 型:一例以胎儿腹水和快速进展性心脏表现为首发表现的新生儿病例报告。
BMC Med Genet. 2020 Feb 19;21(1):37. doi: 10.1186/s12881-020-0972-y.
3
Molecular analysis of mucopolysaccharidosis type VI in Poland, Belarus, Lithuania and Estonia.波兰、白俄罗斯、立陶宛和爱沙尼亚的黏多糖贮积症 VI 型的分子分析。
Mol Genet Metab. 2012 Feb;105(2):237-43. doi: 10.1016/j.ymgme.2011.11.003. Epub 2011 Nov 11.
4
Novel mutations of the arylsulphatase B (ARSB) gene in Indian patients with mucopolysaccharidosis type VI.印度黏多糖贮积症 VI 型患者中芳基硫酸酯酶 B(ARSB)基因的新突变
Indian J Med Res. 2015 Oct;142(4):414-25. doi: 10.4103/0971-5916.169201.
5
Attenuated osteoarticular phenotype of type VI mucopolysaccharidosis: a report of four patients and a review of the literature.VI型黏多糖贮积症的骨关节表型减轻:4例患者报告及文献复习
Clin Rheumatol. 2014 May;33(5):725-31. doi: 10.1007/s10067-013-2423-z. Epub 2013 Nov 13.
6
[Analysis of clinical features and arylsulfatase B gene mutation in thirteen Chinese children with mucopolysaccharidosis type VI].[13例中国黏多糖贮积症Ⅵ型患儿临床特征及芳基硫酸酯酶B基因突变分析]
Zhonghua Er Ke Za Zhi. 2014 Jun;52(6):403-8.
7
Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations.17 例黏多糖贮积症 VI 型患者的临床表现及 8 种新型 ARSB 突变。
Am J Med Genet A. 2014 Jun;164A(6):1443-53. doi: 10.1002/ajmg.a.36489. Epub 2014 Mar 27.
8
Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome) with a predominantly cardiac phenotype.黏多糖贮积症 VI 型(马罗托克斯-拉米综合征),主要表现为心脏表型。
Mol Genet Metab. 2011 Dec;104(4):695-9. doi: 10.1016/j.ymgme.2011.08.024. Epub 2011 Aug 27.
9
Mucopolysaccharidosis type VI (MPS VI) and molecular analysis: Review and classification of published variants in the ARSB gene.黏多糖贮积症 VI 型(MPS VI)及分子分析:ARSB 基因已发表变异的综述和分类。
Hum Mutat. 2018 Dec;39(12):1788-1802. doi: 10.1002/humu.23613. Epub 2018 Sep 17.
10
ARSB gene variants causing Mucopolysaccharidosis VI in Miniature Pinscher and Miniature Schnauzer dogs.导致迷你雪纳瑞和迷你笃宾犬黏多糖贮积症 VI 的 ARSB 基因变异。
Anim Genet. 2020 Dec;51(6):982-986. doi: 10.1111/age.13005. Epub 2020 Sep 28.

引用本文的文献

1
Metabolic Cardiomyopathies and Cardiac Defects in Inherited Disorders of Carbohydrate Metabolism: A Systematic Review.遗传性碳水化合物代谢紊乱相关的代谢性心肌病和心脏缺陷:系统综述。
Int J Mol Sci. 2023 May 11;24(10):8632. doi: 10.3390/ijms24108632.
2
Comparison of growth dynamics in different types of MPS: an attempt to explain the causes.不同类型 MPS 生长动态的比较:原因初探。
Orphanet J Rare Dis. 2022 Sep 5;17(1):339. doi: 10.1186/s13023-022-02486-4.
3
Mucopolysaccharidosis type VI: case report with first neonatal presentation with ascites fetalis and rapidly progressive cardiac manifestation.
黏多糖贮积症 VI 型:一例以胎儿腹水和快速进展性心脏表现为首发表现的新生儿病例报告。
BMC Med Genet. 2020 Feb 19;21(1):37. doi: 10.1186/s12881-020-0972-y.
4
The clinical and genetic Spectrum of Maroteaux-Lamy syndrome (Mucopolysaccharidosis VI) in the Eastern Province of Saudi Arabia.沙特阿拉伯东部省份马罗托-拉米综合征(黏多糖贮积症VI型)的临床与基因谱
J Community Genet. 2018 Jan;9(1):65-70. doi: 10.1007/s12687-017-0329-1. Epub 2017 Sep 15.
5
Recurrent Rare Genomic Copy Number Variants and Bicuspid Aortic Valve Are Enriched in Early Onset Thoracic Aortic Aneurysms and Dissections.复发性罕见基因组拷贝数变异和二叶式主动脉瓣在早发性胸主动脉瘤和夹层中更为常见。
PLoS One. 2016 Apr 19;11(4):e0153543. doi: 10.1371/journal.pone.0153543. eCollection 2016.
6
Human pulmonary artery endothelial cells in the model of mucopolysaccharidosis VI present a prohypertensive phenotype.在黏多糖贮积症VI模型中的人肺动脉内皮细胞呈现出高血压表型。
Mol Genet Metab Rep. 2015 Feb 28;3:11-7. doi: 10.1016/j.ymgmr.2015.02.003. eCollection 2015 Jun.
7
Factors and processes modulating phenotypes in neuronopathic lysosomal storage diseases.调节神经元病变性溶酶体贮积病表型的因素和过程。
Metab Brain Dis. 2014 Mar;29(1):1-8. doi: 10.1007/s11011-013-9455-6. Epub 2013 Dec 5.
8
Attenuated osteoarticular phenotype of type VI mucopolysaccharidosis: a report of four patients and a review of the literature.VI型黏多糖贮积症的骨关节表型减轻:4例患者报告及文献复习
Clin Rheumatol. 2014 May;33(5):725-31. doi: 10.1007/s10067-013-2423-z. Epub 2013 Nov 13.