• 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

犬类神经病:人类遗传性感觉神经病的有力自发模型。

Canine neuropathies: powerful spontaneous models for human hereditary sensory neuropathies.

机构信息

Univ Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR6290, 35000, Rennes, France.

Cancer Genetics and Comparative Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, 20892, USA.

出版信息

Hum Genet. 2019 May;138(5):455-466. doi: 10.1007/s00439-019-02003-x. Epub 2019 Apr 6.

DOI:10.1007/s00439-019-02003-x
PMID:30955094
Abstract

In humans, hereditary sensory neuropathies (HSN), also known as hereditary sensory and autonomic neuropathies (HSAN), constitute a clinically and genetically heterogeneous group of disorders characterized by progressive sensory loss, often accompanied by chronic skin ulcerations and nail dystrophic changes. To date, although around 20 genes have already been discovered, they do not explain the genetic causes of all patients. In dogs, similar neuropathies are also diagnosed, several breeds being predisposed to specific forms of the disease. Indeed, the breed specificity of most canine genetic diseases is due to the small numbers of founders and high levels of inbreeding. Recent knowledge and tools developed to study the canine genome efficiently allows deciphering the genetic bases of such diseases. To date, a dozen breeds are recognized to develop specific HSN. For the Border collie and hunting dog breeds, the genes involved have recently been discovered. Other affected breeds thus constitute potential genetic models, with new genes to be found in dogs that can be considered as candidate genes for human HSAN/HSN. Here, we review the different forms of human and canine HSAN/HSN and we present a novel form in Fox terrier cases, highlighting the advantages of the dog model for such rare human diseases.

摘要

在人类中,遗传性感觉神经病(HSN),也称为遗传性感觉和自主神经病(HSAN),是一组临床和遗传上具有异质性的疾病,其特征为进行性感觉丧失,常伴有慢性皮肤溃疡和指甲营养不良变化。迄今为止,尽管已经发现了约 20 个基因,但它们并不能解释所有患者的遗传原因。在狗中,也诊断出类似的神经病,几种品种易患特定形式的疾病。事实上,大多数犬遗传疾病的品种特异性是由于数量较少的创始人以及高水平的近亲繁殖。最近开发的用于有效研究犬基因组的知识和工具允许破译这些疾病的遗传基础。迄今为止,已有十几种品种被认为会出现特定的 HSN。对于边境牧羊犬和猎犬品种,最近发现了涉及的基因。其他受影响的品种因此构成了潜在的遗传模型,在可被视为人类 HSAN/HSN 候选基因的狗中会发现新的基因。在这里,我们回顾了人类和犬科 HSN/HSN 的不同形式,并介绍了 Fox terrier 病例中的一种新形式,突出了犬模型在这些罕见的人类疾病中的优势。

相似文献

1
Canine neuropathies: powerful spontaneous models for human hereditary sensory neuropathies.犬类神经病:人类遗传性感觉神经病的有力自发模型。
Hum Genet. 2019 May;138(5):455-466. doi: 10.1007/s00439-019-02003-x. Epub 2019 Apr 6.
2
Hereditary sensory and autonomic neuropathy in a family of mixed breed dogs associated with a novel RETREG1 variant.遗传性感觉和自主神经病在一个混种犬家族中与一种新的 RETREG1 变异相关。
J Vet Intern Med. 2021 Sep;35(5):2306-2314. doi: 10.1111/jvim.16242. Epub 2021 Aug 13.
3
A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies.胶质细胞源性神经营养因子(GDNF)上游长链非编码RNA(lincRNA)中的一个点突变与犬类痛觉不敏感相关:一种人类感觉神经病变的自发模型。
PLoS Genet. 2016 Dec 29;12(12):e1006482. doi: 10.1371/journal.pgen.1006482. eCollection 2016 Dec.
4
Disease mechanisms in hereditary sensory and autonomic neuropathies.遗传性感觉和自主神经病变的发病机制
Neurobiol Dis. 2006 Feb;21(2):247-55. doi: 10.1016/j.nbd.2005.08.004. Epub 2005 Sep 23.
5
Two mixed breed dogs with sensory neuropathy are homozygous for an inversion disrupting FAM134B previously identified in Border Collies.两只患有感觉神经病变的混种犬对于先前在边境牧羊犬中发现的一种破坏FAM134B基因的倒位是纯合子。
J Vet Intern Med. 2018 Nov;32(6):2082-2087. doi: 10.1111/jvim.15312. Epub 2018 Oct 11.
6
Natural models for retinitis pigmentosa: progressive retinal atrophy in dog breeds.视网膜色素变性的自然模型:犬种的进行性视网膜萎缩。
Hum Genet. 2019 May;138(5):441-453. doi: 10.1007/s00439-019-01999-6. Epub 2019 Mar 23.
7
Hereditary sensory and autonomic neuropathies.遗传性感觉和自主神经病
Handb Clin Neurol. 2013;115:893-906. doi: 10.1016/B978-0-444-52902-2.00050-3.
8
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies.先天性痛觉缺失和遗传性感觉和自主神经病的遗传景观。
Brain. 2023 Dec 1;146(12):4880-4890. doi: 10.1093/brain/awad328.
9
Hereditary sensory neuropathies.
Drugs Today (Barc). 2004 May;40(5):385-94. doi: 10.1358/dot.2004.40.5.850487.
10
Molecular pathogenesis, experimental therapy and genetic counseling in hereditary sensory neuropathies.遗传性感觉神经病的分子发病机制、实验性治疗及遗传咨询
Acta Neurobiol Exp (Wars). 2015;75(2):126-43. doi: 10.55782/ane-2015-2023.

引用本文的文献

1
A diffusion tensor imaging white matter atlas of the domestic canine brain.家犬脑的扩散张量成像白质图谱。
Imaging Neurosci (Camb). 2024 Aug 30;2:1-21. doi: 10.1162/imag_a_00276. eCollection 2024 Aug 1.
2
An Overview of Canine Inherited Neurological Disorders with Known Causal Variants.已知致病变异的犬遗传性神经疾病概述
Animals (Basel). 2023 Nov 18;13(22):3568. doi: 10.3390/ani13223568.
3
SCN9A variant in a family of mixed breed dogs with congenital insensitivity to pain.一个混血犬家族中存在 SCN9A 变异,该家族患有先天性痛觉缺失症。

本文引用的文献

1
Juvenile-onset polyneuropathy in American Staffordshire Terriers.美国斯塔福郡梗犬的幼年型多发性神经病。
J Vet Intern Med. 2018 Nov;32(6):2003-2012. doi: 10.1111/jvim.15316. Epub 2018 Oct 13.
2
MKLN1 splicing defect in dogs with lethal acrodermatitis.犬致死性肢端皮炎中 MKLN1 的剪接缺陷。
PLoS Genet. 2018 Mar 22;14(3):e1007264. doi: 10.1371/journal.pgen.1007264. eCollection 2018 Mar.
3
Demographic history, selection and functional diversity of the canine genome.犬科基因组的人口历史、选择和功能多样性。
J Vet Intern Med. 2023 Jan;37(1):230-235. doi: 10.1111/jvim.16610. Epub 2023 Jan 11.
4
A comprehensive review of genomic perspectives of canine diseases as a model to study human disorders.犬类疾病的基因组视角综述:作为研究人类疾病的模型
Can J Vet Res. 2023 Jan;87(1):3-8.
5
Inheritance of Monogenic Hereditary Skin Disease and Related Canine Breeds.单基因遗传性皮肤病的遗传与相关犬种
Vet Sci. 2022 Aug 15;9(8):433. doi: 10.3390/vetsci9080433.
6
Role of animal models in biomedical research: a review.动物模型在生物医学研究中的作用:综述
Lab Anim Res. 2022 Jul 1;38(1):18. doi: 10.1186/s42826-022-00128-1.
7
Inherited Sensory and Autonomic Neuropathy in a Border Collie, Interest of Oclacitinib for the Control of Self-Mutilation.一只边境牧羊犬的遗传性感觉和自主神经病变,奥克拉替尼对控制自残行为的作用
Vet Sci. 2022 Mar 10;9(3):127. doi: 10.3390/vetsci9030127.
8
Hereditary sensory and autonomic neuropathy in a family of mixed breed dogs associated with a novel RETREG1 variant.遗传性感觉和自主神经病在一个混种犬家族中与一种新的 RETREG1 变异相关。
J Vet Intern Med. 2021 Sep;35(5):2306-2314. doi: 10.1111/jvim.16242. Epub 2021 Aug 13.
9
Myocardial ischaemia reperfusion injury and cardioprotection in the presence of sensory neuropathy: Therapeutic options.感觉神经病变情况下的心肌缺血再灌注损伤与心脏保护:治疗选择
Br J Pharmacol. 2020 Dec;177(23):5336-5356. doi: 10.1111/bph.15021. Epub 2020 Mar 21.
10
Special issue on canine genetics: animal models for human disease and gene therapies, new discoveries for canine inherited diseases, and standards and guidelines for clinical genetic testing for domestic dogs.犬类遗传学特刊:人类疾病和基因治疗的动物模型、犬类遗传性疾病的新发现以及家犬临床基因检测的标准和指南。
Hum Genet. 2019 May;138(5):437-440. doi: 10.1007/s00439-019-02025-5. Epub 2019 May 5.
Nat Rev Genet. 2017 Dec;18(12):705-720. doi: 10.1038/nrg.2017.67. Epub 2017 Sep 25.
4
A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs.一种GJA9移码变异与圣伯纳犬的多发性神经病相关。
BMC Genomics. 2017 Aug 25;18(1):662. doi: 10.1186/s12864-017-4081-z.
5
ARL6IP1 mutation causes congenital insensitivity to pain, acromutilation and spastic paraplegia.ARL6IP1 突变导致先天性无痛症、肢端肥大和痉挛性截瘫。
Clin Genet. 2018 Jan;93(1):169-172. doi: 10.1111/cge.13048. Epub 2017 Aug 31.
6
FEELnc: a tool for long non-coding RNA annotation and its application to the dog transcriptome.FEELnc:一种用于长链非编码RNA注释的工具及其在犬转录组中的应用。
Nucleic Acids Res. 2017 May 5;45(8):e57. doi: 10.1093/nar/gkw1306.
7
A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies.胶质细胞源性神经营养因子(GDNF)上游长链非编码RNA(lincRNA)中的一个点突变与犬类痛觉不敏感相关:一种人类感觉神经病变的自发模型。
PLoS Genet. 2016 Dec 29;12(12):e1006482. doi: 10.1371/journal.pgen.1006482. eCollection 2016 Dec.
8
Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception.血红素转运蛋白FLVCR1的突变导致感觉神经退行性变并丧失痛觉。
PLoS Genet. 2016 Dec 6;12(12):e1006461. doi: 10.1371/journal.pgen.1006461. eCollection 2016 Dec.
9
An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed.一种破坏FAM134B的倒位与边境牧羊犬品种的感觉神经病变有关。
G3 (Bethesda). 2016 Sep 8;6(9):2687-92. doi: 10.1534/g3.116.027896.
10
Classifications of neurogenetic diseases: An increasingly complex problem.神经遗传性疾病的分类:一个日益复杂的问题。
Rev Neurol (Paris). 2016 Jun-Jul;172(6-7):339-49. doi: 10.1016/j.neurol.2016.04.005. Epub 2016 May 27.