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Insights into Pathomechanisms and Treatment Development in Heritable Ectopic Mineralization Disorders: Summary of the PXE International Biennial Research Symposium—2016

机译:对遗传性异位矿化疾病的发病机理和治疗进展的见解:PXE国际双年研究研讨会—2016年摘要

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摘要

Pseudoxanthoma elasticum is a prototype of heritable ectopic mineralization disorders, with phenotypic overlap with generalized arterial calcification of infancy and arterial calcification due to CD73 deficiency. Recent observations have suggested that the reduced inorganic pyrophosphate/phosphate ratio is the cause of soft connective tissue mineralization in these disorders. PXE International, a patient advocacy organization, supports research in part by sponsoring biennial research symposia on these disorders; the latest meeting was held in September 2016 at Thomas Jefferson University, Philadelphia. This report summarizes the progress in pseudoxanthoma elasticum and other ectopic mineralization disorders, as presented in the symposium, with focus on translational aspects of precision medicine toward improved diagnostics and treatment development for these currently intractable disorders.
机译:弹性假黄瘤是遗传性异位矿化疾病的原型,表型重叠,婴儿期全身动脉钙化和CD73缺乏引起动脉钙化。最近的观察表明,降低的无机焦磷酸盐/磷酸盐比率是这些疾病中软结缔组织矿化的原因。患者倡导组织PXE International通过赞助关于这些疾病的两年期研究专题讨论会来部分支持研究;最近一次会议于2016年9月在费城的托马斯·杰斐逊大学举行。该报告总结了研讨会上介绍的弹性假黄瘤和其他异位矿化疾病的进展,重点是精密医学的翻译方面,以改善这些目前难治性疾病的诊断和治疗开发水平。

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