A 6-year-old girl with parsonage-turner syndrome: A mysterious case of sudden bilateral arm weakness, a case report

Sikandar Ajmal Abbasi , Muhammad Usama bin Shabbir , Siham Alshawamreh , Daniya Jawed , Kamran khan , Mohsin Abbas
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Abstract

Parsonage-Turner Syndrome is a rare idiopathic neurological condition characterized by acute shoulder pain, arm and shoulder atrophy, and muscle weakness. PTS is uncommon, has a wide range of clinical presentations, makes diagnosis difficult, and has no established course of treatment. Here, we present a case of a 6-year-old female diagnosed with bilateral brachial plexus pan plexopathy and PTS. Initial symptoms included acute shoulder pain and subsequent motor deficits in both arms, with no recognized mechanism of damage. The treatment difficulties and clinical complexity related to pediatric PTS are highlighted in this case report. To improve knowledge of the condition's various clinical manifestations, therapeutic responses, and long-term consequences, it is imperative to document such cases.
一个患有牧师-特纳综合征的6岁女孩:一个神秘的突然双侧手臂无力的病例报告
帕森纳-特纳综合征是一种罕见的特发性神经系统疾病,其特征是急性肩部疼痛,手臂和肩部萎缩以及肌肉无力。PTS是罕见的,有广泛的临床表现,使诊断困难,并没有确定的治疗过程。在这里,我们提出一个6岁的女性诊断为双侧臂丛泛神经丛病和PTS。最初的症状包括急性肩部疼痛和随后的双臂运动障碍,没有明确的损伤机制。本病例报告强调了小儿PTS的治疗困难和临床复杂性。为了提高对这种疾病的各种临床表现、治疗反应和长期后果的认识,有必要记录这些病例。
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