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Ring Finger Protein 213 in Moyamoya Disease With Pulmonary Arterial Hypertension: A Mini-Review

Moyamoya disease (MMD), most often diagnosed in children and adolescents, is a chronic cerebrovascular disease characterized by progressive stenosis at the terminal portion of the internal carotid artery and an abnormal vascular network at the base of the brain. Recently, many investigators show a g...

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Autores principales: Luo, Yuting, Cao, Zhixin, Wu, Shaoqing, Sun, Xunsha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8987108/
https://www.ncbi.nlm.nih.gov/pubmed/35401401
http://dx.doi.org/10.3389/fneur.2022.843927
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author Luo, Yuting
Cao, Zhixin
Wu, Shaoqing
Sun, Xunsha
author_facet Luo, Yuting
Cao, Zhixin
Wu, Shaoqing
Sun, Xunsha
author_sort Luo, Yuting
collection PubMed
description Moyamoya disease (MMD), most often diagnosed in children and adolescents, is a chronic cerebrovascular disease characterized by progressive stenosis at the terminal portion of the internal carotid artery and an abnormal vascular network at the base of the brain. Recently, many investigators show a great interest in MMD with pulmonary arterial hypertension (PAH). Ring finger protein 213 (RNF213) is a major susceptibility gene for MMD and also has strong correlations with PAH. Therefore, this review encapsulates current cases of MMD with PAH and discusses MMD with PAH in the aspects of epidemiology, pathology, possible pathogenesis, clinical manifestations, diagnosis, and treatment.
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spelling pubmed-89871082022-04-08 Ring Finger Protein 213 in Moyamoya Disease With Pulmonary Arterial Hypertension: A Mini-Review Luo, Yuting Cao, Zhixin Wu, Shaoqing Sun, Xunsha Front Neurol Neurology Moyamoya disease (MMD), most often diagnosed in children and adolescents, is a chronic cerebrovascular disease characterized by progressive stenosis at the terminal portion of the internal carotid artery and an abnormal vascular network at the base of the brain. Recently, many investigators show a great interest in MMD with pulmonary arterial hypertension (PAH). Ring finger protein 213 (RNF213) is a major susceptibility gene for MMD and also has strong correlations with PAH. Therefore, this review encapsulates current cases of MMD with PAH and discusses MMD with PAH in the aspects of epidemiology, pathology, possible pathogenesis, clinical manifestations, diagnosis, and treatment. Frontiers Media S.A. 2022-03-24 /pmc/articles/PMC8987108/ /pubmed/35401401 http://dx.doi.org/10.3389/fneur.2022.843927 Text en Copyright © 2022 Luo, Cao, Wu and Sun. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Luo, Yuting
Cao, Zhixin
Wu, Shaoqing
Sun, Xunsha
Ring Finger Protein 213 in Moyamoya Disease With Pulmonary Arterial Hypertension: A Mini-Review
title Ring Finger Protein 213 in Moyamoya Disease With Pulmonary Arterial Hypertension: A Mini-Review
title_full Ring Finger Protein 213 in Moyamoya Disease With Pulmonary Arterial Hypertension: A Mini-Review
title_fullStr Ring Finger Protein 213 in Moyamoya Disease With Pulmonary Arterial Hypertension: A Mini-Review
title_full_unstemmed Ring Finger Protein 213 in Moyamoya Disease With Pulmonary Arterial Hypertension: A Mini-Review
title_short Ring Finger Protein 213 in Moyamoya Disease With Pulmonary Arterial Hypertension: A Mini-Review
title_sort ring finger protein 213 in moyamoya disease with pulmonary arterial hypertension: a mini-review
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8987108/
https://www.ncbi.nlm.nih.gov/pubmed/35401401
http://dx.doi.org/10.3389/fneur.2022.843927
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