Division of Child Neurology, University of Texas Southwestern, Dallas, TX 75390, USA.
Genes (Basel). 2024 Jan 27;15(2):171. doi: 10.3390/genes15020171.
The progressive myoclonus epilepsies (PME) are a diverse group of disorders that feature both myoclonus and seizures that worsen gradually over a variable timeframe. While each of the disorders is individually rare, they collectively make up a non-trivial portion of the complex epilepsy and myoclonus cases that are seen in tertiary care centers. The last decade has seen substantial progress in our understanding of the pathophysiology, diagnosis, prognosis, and, in select disorders, therapies of these diseases. In this scoping review, we examine English language publications from the past decade that address diagnostic, phenotypic, and therapeutic advances in all PMEs. We then highlight the major lessons that have been learned and point out avenues for future investigation that seem promising.
进行性肌阵挛性癫痫(PME)是一组多种疾病的统称,这些疾病都具有肌阵挛和癫痫发作,且在不同时间段逐渐加重。虽然每种疾病都很少见,但它们共同构成了三级护理中心中复杂癫痫和肌阵挛病例的重要部分。在过去的十年中,我们对这些疾病的病理生理学、诊断、预后以及在某些疾病中的治疗方法有了实质性的了解。在这篇范围综述中,我们检查了过去十年中发表的英语文献,这些文献涉及所有 PME 的诊断、表型和治疗进展。然后,我们强调了已经学到的主要经验教训,并指出了未来有希望的研究方向。