Ring Finger Protein 213 in Moyamoya Disease With Pulmonary Arterial Hypertension: A Mini-Review
Open Access
- 24 March 2022
- journal article
- review article
- Published by Frontiers Media SA in Frontiers in Neurology
- Vol. 13, 843927
Abstract
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.Keywords
Funding Information
- National Natural Science Foundation of China (81102248, 81601004, 82071292)
- National Natural Science Foundation of China-Guangdong Joint Fund (2016A030310139)
- Fundamental Research Funds for the Central Universities (20ykpy66)
This publication has 91 references indexed in Scilit:
- Elastic fibres in health and diseaseExpert Reviews in Molecular Medicine, 2013
- Fatal outcomes of pediatric patients with moyamoya disease associated with pulmonary arterial hypertension. Report of two casesClinical Neurology and Neurosurgery, 2013
- RNF213 polymorphism and Moyamoya disease: A systematic review and meta-analysisNeurology India, 2013
- Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya diseaseNeurology, 2012
- Identification of RNF213 as a Susceptibility Gene for Moyamoya Disease and Its Possible Role in Vascular DevelopmentPLOS ONE, 2011
- Discrete Contributions of Elastic Fiber Components to Arterial Development and Mechanical ComplianceArteriosclerosis, Thrombosis, and Vascular Biology, 2009
- Vascular Permeability and Pathological Angiogenesis in Caveolin-1-Null MiceThe American Journal of Pathology, 2009
- Loss of Caveolae, Vascular Dysfunction, and Pulmonary Defects in Caveolin-1 Gene-Disrupted MiceScience, 2001
- Renovascular hypertension in children with moyamoya diseaseThe Journal of Pediatrics, 1997
- Smooth muscle cell proliferation and localization of macrophages and T cells in the occlusive intracranial major arteries in moyamoya disease.Stroke, 1993