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Eighth International Chorea–Acanthocytosis Symposium: Summary of Workshop Discussion and Action Points

机译:第八届国际Chrea–Acanthocytosis研讨会:研讨会讨论和行动要点摘要

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摘要

Chorea-Acanthocytosis (ChAc) is a rare hereditary neurological disorder characterized by abnormal movements, red blood cell pathology, and progressive neurodegeneration. Little is understood of the pathogenesis of ChAc and related disorders (collectively Neuroacanthocytosis). The Eighth International Chorea-Acanthocytosis Symposium was held in May 2016 in Ann Arbor, MI, USA, and focused on molecular mechanisms driving ChAc pathophysiology. Accompanying the meeting, members of the neuroacanthocytosis research community and other invited scientists met in a workshop to discuss the current understanding and next steps needed to better understand ChAc pathogenesis. These discussions identified several broad and critical needs for advancing ChAc research and patient care, and led to the definition of 18 specific action points related to functional and molecular studies, animal models, and clinical research. These action points, described below, represent tractable research goals to pursue for the next several years.
机译:Chorea-Acanthocytosis(ChAc)是一种罕见的遗传性神经系统疾病,其特征在于运动异常,红细胞病理和进行性神经变性。人们对ChAc和相关疾病(统称为神经棘皮细胞增多症)的发病机理了解甚少。第八届国际Chrea-Acanthocytosis研讨会于2016年5月在美国密歇根州安阿伯市举行,主题是驱动ChAc病理生理的分子机制。伴随会议,神经棘皮细胞增多症研究社区的成员和其他受邀科学家参加了研讨会,讨论了当前的理解以及更好地了解ChAc发病机理所需的下一步。这些讨论确定了推进ChAc研究和患者护理的几个广泛且关键的需求,并导致了18个与功能和分子研究,动物模型和临床研究有关的特定作用点的定义。这些行动要点,如下所述,代表了未来几年要追求的可预测的研究目标。

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