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1.
Chinese Medical Journal ; (24): 2497-2501, 2016.
Article in English | WPRIM | ID: wpr-307386

ABSTRACT

<p><b>OBJECTIVE</b>The aim of this study was to help people comprehensively understand the research advances related to ring finger protein 213 (RNF213) in moyamoya disease (MMD) and to understand the disease at the molecular level to provide a new perspective of the diagnosis of the disease.</p><p><b>DATA SOURCES</b>This review was based on data in articles published between 2005 and 2015 that were retrieved from the PubMed database. The search terms included RNF213, MMD, intracranial major artery stenosis /occlusion (ICASO), genotype, phenotype, mutant and variants, and the combinations of these terms.</p><p><b>STUDY SELECTION</b>Articles related to MMD and RNF213 were selected for review, and we also reviewed publications related to ICASO.</p><p><b>RESULTS</b>RNF213 is not only associated with MMD but also associated with intracranial major artery stenosis. In addition, RNF213 variants exhibit apparent ethnic diversity; specifically, the c.14576G>A variant is mainly detected in Korean, Chinese, and Japanese populations, particularly the latter population. The genotypes of RNF213 correlate with the phenotypes of MMD; for example, the homozygous c.14576G>A variant is associated with early-onset, severe symptoms, and an unfavorable prognosis. Furthermore, the RNF213 c.14576G>A variant should be considered during the diagnosis of MMD because no patients with quasi-MMD have been reported to carry the RNF213 c.14576G>A variant whereas 66 of 78 patients with definite MMD have been found to carry this variant.</p><p><b>CONCLUSIONS</b>The growing literature demonstrates that MMD is primarily caused by the synergy of genetic and environmental factors, and unknown genetic modifiers might play roles in the etiology of MMD. Further research should be conducted to clarify the pathogenic mechanism of MMD.</p>


Subject(s)
Animals , Humans , Adenosine Triphosphatases , Genetics , Asian People , Genetic Predisposition to Disease , Genotype , Moyamoya Disease , Genetics , Phenotype , Ubiquitin-Protein Ligases , Genetics
2.
Chinese Medical Journal ; (24): 3231-3237, 2015.
Article in English | WPRIM | ID: wpr-275533

ABSTRACT

<p><b>OBJECTIVE</b>To introduce the imaging characteristics of moyamoya disease (MMD) using high-resolution magnetic resonance imaging (HR-MRI) and to discuss the role of HR-MRI in differentiating MMD from other intracranial artery diseases, especially intracranial atherosclerotic disease (ICAD).</p><p><b>DATA SOURCES</b>This review was based on the data in articles published between 2005 and 2015, which were obtained from PubMed. The keywords included HR-MRI, MMD, ICAD, and intracranial artery diseases.</p><p><b>STUDY SELECTION</b>Articles related to HR-MRI for MMD or other intracranial artery diseases were selected for review.</p><p><b>RESULTS</b>There are differences between the characteristic patterns of HR-MRI in MMD and ICAD. MMD is associated with inward remodeling, smaller outer diameters, concentric occlusive lesions and homogeneous signal intensity, while ICAD is more likely to be associated with outward remodeling, normal outer diameters, eccentric occlusive lesions, and heterogeneous signal intensity. Other intracranial artery diseases, such as dissection and vasculitis, also have distinctive characteristics in HR-MRI. HR-MRI may become a useful tool for the differential diagnosis of MMD in the future.</p><p><b>CONCLUSIONS</b>HR-MRI of MMD provides a more in-depth understanding of MMD, and it is helpful in evaluating pathological changes in the vessel wall and in differentiating MMD from other intracranial artery steno-occlusive diseases, particularly ICAD.</p>


Subject(s)
Animals , Humans , Diagnosis, Differential , Magnetic Resonance Imaging , Methods , Middle Cerebral Artery , Pathology , Moyamoya Disease , Diagnosis
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