Peripheral circulation disturbances in two consecutive children with spinal muscular atrophy and literature review.

Q3 Medicine Acta Myologica Pub Date : 2022-06-30 eCollection Date: 2022-06-01 DOI:10.36185/2532-1900-072
Gloria Cristofano, Martina Fucci, Maria Carmela Oliva, Marta De Rinaldis, Antonio Trabacca
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Abstract

Spinal muscular atrophy is a progressive and severe hereditary (autosomal recessive) neuromuscular disease characterized by lower motor neuron degeneration in the spinal cord and brainstem causing a clinical picture of progressive muscle atrophy and weakness of skeletal and respiratory muscles. There is an ongoing discussion on the extent to which other tissues might be affected in patients with SMA. Several animal models and some case reports or small case series report involvement of other organ systems, such as peripheral nerve, brain, muscle, heart, vascular system, and pancreas. Recent literature reviews identified a number of cases with vascular abnormalities. We present two consecutive cases of patients diagnosed with SMA who developed peripheral circulation disturbances and combine the findings with a thorough review the literature.

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连续2例脊髓性肌萎缩症患儿外周血循环障碍及文献复习。
脊髓性肌萎缩是一种进行性和严重的遗传性(常染色体隐性)神经肌肉疾病,其特征是脊髓和脑干下部运动神经元变性,导致进行性肌肉萎缩和骨骼肌和呼吸肌无力的临床表现。关于SMA患者的其他组织可能受影响的程度,目前正在进行讨论。一些动物模型和一些病例报告或小病例系列报告称累及其他器官系统,如周围神经、脑、肌肉、心脏、血管系统和胰腺。最近的文献综述发现了一些血管异常的病例。我们提出了两个连续的病例,患者诊断为肌萎缩症谁发展外周循环障碍,并结合研究结果与彻底回顾文献。
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来源期刊
Acta Myologica
Acta Myologica Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.70
自引率
0.00%
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0
期刊最新文献
PROCEEDINGS OF THE XXIII CONGRESS OF THE ITALIAN ASSOCIATION OF MYOLOGY: PadovaJune 8-10, 2023. Year 2023: a new look for Acta Myologica. Experience with telemedicine in neuromuscular clinic during COVID-19 pandemic. VCP-related myopathy: a case series and a review of literature. Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.
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