Arrhythmogenic Right Ventricular Dysplasia

"Arrhythmogenic Right Ventricular Dysplasia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

A congenital cardiomyopathy that is characterized by infiltration of adipose and fibrous tissue into the RIGHT VENTRICLE wall and loss of myocardial cells. Primary injuries usually are at the free wall of right ventricular and right atria resulting in ventricular and supraventricular arrhythmias.

Descriptor ID	D019571
MeSH Number(s)	C14.240.400.145 C14.280.238.028 C14.280.400.145 C16.131.240.400.145
Concept/Terms	Arrhythmogenic Right Ventricular Dysplasia Arrhythmogenic Right Ventricular Dysplasia Arrhythmogenic Right Ventricular Cardiomyopathy-Dysplasia Arrhythmogenic Right Ventricular Cardiomyopathy Dysplasia Ventricular Dysplasia, Right, Arrhythmogenic ARVD-C Right Ventricular Dysplasia, Arrhythmogenic Arrhythmogenic Right Ventricular Cardiomyopathy Arrhythmogenic Right Ventricular Dysplasia-Cardiomyopathy

Below are MeSH descriptors whose meaning is more general than "Arrhythmogenic Right Ventricular Dysplasia".

Diseases [C]
Cardiovascular Diseases [C14]
Cardiovascular Abnormalities [C14.240]
Heart Defects, Congenital [C14.240.400]
Arrhythmogenic Right Ventricular Dysplasia [C14.240.400.145]
Heart Diseases [C14.280]
Cardiomyopathies [C14.280.238]
Arrhythmogenic Right Ventricular Dysplasia [C14.280.238.028]
Heart Defects, Congenital [C14.280.400]
Arrhythmogenic Right Ventricular Dysplasia [C14.280.400.145]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Cardiovascular Abnormalities [C16.131.240]
Heart Defects, Congenital [C16.131.240.400]
Arrhythmogenic Right Ventricular Dysplasia [C16.131.240.400.145]

Below are MeSH descriptors whose meaning is related to "Arrhythmogenic Right Ventricular Dysplasia".

Below are MeSH descriptors whose meaning is more specific than "Arrhythmogenic Right Ventricular Dysplasia".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Arrhythmogenic Right Ventricular Dysplasia" by people in this website by year, and whether "Arrhythmogenic Right Ventricular Dysplasia" was a major or minor topic of these publications.

Bar chart showing 12 publications over 9 distinct years, with a maximum of 2 publications in 2006 and 2017 and 2019

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2003	1	0	1
2004	0	1	1
2006	2	0	2
2009	1	0	1
2010	1	0	1
2017	2	0	2
2018	1	0	1
2019	2	0	2
2022	1	0	1

Below are the most recent publications written about "Arrhythmogenic Right Ventricular Dysplasia" by people in Profiles.

Rouhi L, Fan S, Cheedipudi SM, Braza-Boïls A, Molina MS, Yao Y, Robertson MJ, Coarfa C, Gimeno JR, Molina P, Gurha P, Zorio E, Marian AJ. The EP300/TP53 pathway, a suppressor of the Hippo and canonical WNT pathways, is activated in human hearts with arrhythmogenic cardiomyopathy in the absence of overt heart failure. Cardiovasc Res. 2022 05 06; 118(6):1466-1478.

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Hall CL, Gurha P, Sabater-Molina M, Asimaki A, Futema M, Lovering RC, Suárez MP, Aguilera B, Molina P, Zorio E, Coarfa C, Robertson MJ, Cheedipudi SM, Ng KE, Delaney P, Hernández JP, Pastor F, Gimeno JR, McKenna WJ, Marian AJ, Syrris P. RNA sequencing-based transcriptome profiling of cardiac tissue implicates novel putative disease mechanisms in FLNC-associated arrhythmogenic cardiomyopathy. Int J Cardiol. 2020 03 01; 302:124-130.

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Headrick AT, Rosenfeld JA, Yang Y, Tunuguntla H, Allen HD, Penny DJ, Kim JJ, Landstrom AP. Incidentally identified genetic variants in arrhythmogenic right ventricular cardiomyopathy-associated genes among children undergoing exome sequencing reflect healthy population variation. Mol Genet Genomic Med. 2019 06; 7(6):e593.

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Zheng G, Jiang C, Li Y, Yang D, Ma Y, Zhang B, Li X, Zhang P, Hu X, Zhao X, Du J, Lin X. TMEM43-S358L mutation enhances NF-?B-TGFß signal cascade in arrhythmogenic right ventricular dysplasia/cardiomyopathy. Protein Cell. 2019 02; 10(2):104-119.

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Petrovic M, Buja LM, Kar B, Colnaric J, Damaraju S, Zhao B, Akkanti B, Radovanovic M, Radovancevic R, Loyalka P, Gregoric ID. Cardiac sarcoidosis presenting as arrhythmogenic right ventricular cardiomyopathy/dysplasia with ventricular aneurysms: a case report. Cardiovasc Pathol. 2018 Mar - Apr; 33:1-5.

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Karmouch J, Zhou QQ, Miyake CY, Lombardi R, Kretzschmar K, Bannier-Hélaouët M, Clevers H, Wehrens XHT, Willerson JT, Marian AJ. Distinct Cellular Basis for Early Cardiac Arrhythmias, the Cardinal Manifestation of Arrhythmogenic Cardiomyopathy, and the Skin Phenotype of Cardiocutaneous Syndromes. Circ Res. 2017 Dec 08; 121(12):1346-1359.

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Frangogiannis NG. Fibroblasts and the extracellular matrix in right ventricular disease. Cardiovasc Res. 2017 Oct 01; 113(12):1453-1464.

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Xiong Q, Cao Q, Zhou Q, Xie J, Shen Y, Wan R, Yu J, Yan S, Marian AJ, Hong K. Arrhythmogenic cardiomyopathy in a patient with a rare loss-of-function KCNQ1 mutation. J Am Heart Assoc. 2015 Jan 23; 4(1):e001526.

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Chen SN, Gurha P, Lombardi R, Ruggiero A, Willerson JT, Marian AJ. The hippo pathway is activated and is a causal mechanism for adipogenesis in arrhythmogenic cardiomyopathy. Circ Res. 2014 Jan 31; 114(3):454-68.

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Marian AJ. On the diagnostic utility of junction plakoglobin in arrhythmogenic right ventricular cardiomyopathy. Cardiovasc Pathol. 2013 Sep-Oct; 22(5):309-11.

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