RYR1 myopathy complicated by RSV bronchiolitis requiring intubation leading to posthypoxic leukoencephalopathy in a 4 year-old.

Vincent Czerwinski, Shawn Sood, Francesca Perez Marques, Travis Langner, Kelly Dahlstrom, Kyle Summers
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Abstract

Central core disease due to RYR1 mutations is a rare heterogeneous myopathy characterized by skeletal muscle weakness. In light of both the rarity of presentation as well as the relatively broad spectrum of clinical phenotypes, there is a need to report treatment strategies for common complications of this condition. In this case, we outline the ICU management of a 4 year-old girl with central core disease caused by RYR1 mutation who was hospitalized due to respiratory syncytial virus (RSV) bronchiolitis leading to respiratory failure. Her hospital stay was complicated by multiple failed extubations, hospital infections, and post-anoxic leukoencephalopathy.
1例4岁儿童RYR1肌病合并RSV细支气管炎,需要插管导致后毒性脑白质病。
RYR1突变引起的中央核心病是一种罕见的异质性肌病,其特征是骨骼肌无力。鉴于罕见的表现以及相对广泛的临床表型,有必要报告这种情况的常见并发症的治疗策略。在本病例中,我们概述了一名因呼吸道合胞病毒(RSV)毛细支气管炎导致呼吸衰竭而住院的4岁女孩RYR1突变引起的中央核心疾病的ICU管理。她的住院期间因多次拔管失败、医院感染和缺氧后脑白质病而变得复杂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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