Cutaneous manifestations in Moyamoya angiopathy: A review

Mitri Fouad; Bersano Anna; Herve Dominique; Kraemer Markus

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Cutaneous manifestations in Moyamoya angiopathy: A review

机译：Moyamoya Angiocathy的皮肤表现：综述

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Background and purpose: Moyamoya angiopathy (MA) is a progressive cerebrovascular disease with a poorly understood pathophysiology. It is mainly characterized by progressive bilateral stenosis of the terminal intracranial part of the supraclinoid internal carotid arteries and the proximal parts of the middle and anterior cerebral arteries. This results in early-onset ischemic or hemorrhagic strokes. The disease may be idiopathic (known as Moyamoya disease) or associated with other heritable or acquired conditions, including type 1 neurofibromatosis or other RASopathies, sickle cell disease, Down syndrome, or autoimmune disorders (known as Moyamoya syndrome). Apart from the brain, other organ manifestations including cutaneous ones have also been described in MA patients.

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来源
《European journal of neurology: the official journal of the European Federation of Neurological Societies》 |2021年第5期|共10页
作者
Mitri Fouad; Bersano Anna; Herve Dominique; Kraemer Markus;
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作者单位

Univ Hosp Heidelberg Dept Dermatol Neuenheimer Feld 440 D-69120 Heidelberg Germany;

Fdn IRCCS Ist Neurol Carlo Besta Cerebrovasc Unit Milan Italy;

Hop Lariboisiere CERVCO Ctr Reference Malad Vasc Rares Cerveu &

Oe Paris France;

Alfried Krupp von Bohlen &

Halbach Hosp Dept Neurol Essen Germany;

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原文格式 PDF
正文语种 eng
中图分类神经病学;
关键词
cutaneous; hemangioma; livedo; loose hair; Moyamoya; neurofibromatosis; Noonan syndrome;

机译：皮肤;血管瘤;Liveo;松散的头发;Moyamoya;神经纤维瘤病;Noonan综合征;

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Cutaneous manifestations in Moyamoya angiopathy: A review

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