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p.R220L Is a Likely Pathogenic Novel GLA Gene Mutation Responsible for Fabry Disease.

作者信息

Barman Hasan Ali, Atıcı Adem, Özyıldırım Serhan, Ceylaner Serdar, Dursun Memduh, Doğan Sait Mesut

机构信息

Department of Cardiology, İstanbul University-Cerrahpaşa, Institute of Cardiology, İstanbul, Turkey.

Department of Medical Genetics, Intergen Genetic Centre, Ankara, Turkey.

出版信息

Anatol J Cardiol. 2022 May;26(5):411-413. doi: 10.5152/AnatolJCardiol.2021.393.

DOI:10.5152/AnatolJCardiol.2021.393
PMID:35552179
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9366415/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c63a/9366415/10022583afaa/ajc-26-5-411_f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c63a/9366415/e3eb6c151068/ajc-26-5-411_f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c63a/9366415/78faee69e355/ajc-26-5-411_f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c63a/9366415/f8832d7e2618/ajc-26-5-411_f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c63a/9366415/10022583afaa/ajc-26-5-411_f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c63a/9366415/e3eb6c151068/ajc-26-5-411_f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c63a/9366415/78faee69e355/ajc-26-5-411_f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c63a/9366415/f8832d7e2618/ajc-26-5-411_f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c63a/9366415/10022583afaa/ajc-26-5-411_f004.jpg

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p.R220L Is a Likely Pathogenic Novel GLA Gene Mutation Responsible for Fabry Disease.p.R220L是一种可能致病的新型GLA基因突变,与法布里病相关。
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本文引用的文献

1
Ratio of Fabry disease in patients with idiopathic left ventricular hypertrophy: A single-center study in Turkey.特发性左心室肥厚患者中法布里病的比例:土耳其的一项单中心研究。
Anatol J Cardiol. 2020 Jan;23(2):79-85. doi: 10.14744/AnatolJCardiol.2019.84782.
2
Assessment of Cardiac Involvement in Fabry Disease (FD) with Native T1 Mapping.采用原生T1成像评估法布里病(FD)患者的心脏受累情况。
Rofo. 2019 Oct;191(10):932-939. doi: 10.1055/a-0836-2723. Epub 2019 Feb 12.
3
Is it Fabry disease?这是法布里病吗?
Genet Med. 2016 Dec;18(12):1181-1185. doi: 10.1038/gim.2016.55. Epub 2016 May 19.
4
Plasma globotriaosylsphingosine in relation to phenotypes of Fabry disease.与法布里病表型相关的血浆球三糖神经酰胺
J Med Genet. 2015 Apr;52(4):262-8. doi: 10.1136/jmedgenet-2014-102872. Epub 2015 Jan 16.
5
Fabry disease.法布里病。
Orphanet J Rare Dis. 2010 Nov 22;5:30. doi: 10.1186/1750-1172-5-30.
6
Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey.法布里病的定义:法布里病结局调查中366例患者的基线临床表现。
Eur J Clin Invest. 2004 Mar;34(3):236-42. doi: 10.1111/j.1365-2362.2004.01309.x.
7
Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency.法布里病的酶缺陷。神经酰胺三己糖苷酶缺乏症。
N Engl J Med. 1967 May 25;276(21):1163-7. doi: 10.1056/NEJM196705252762101.