Six Years Follow-Up of an 11-Year-Old Girl with Anti-HMGCR Myopathy.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-01-01 DOI:10.3233/JND-240022
Dilek Cavusoglu, Beril Talim, Gazanfer Ekinci, Haluk Topaloglu
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Abstract

Anti-HMGCR myopathy is decribed as an immune-mediated necrotizing myopathy which is characterised by subacute, progressive proximal muscle weakness and elevated creatine kinase (CK) level. In pediatric population, anti-HMGCR myopathy has been reported solely as small case reports, albeit rare. Although treatment consensus has not yet been established, proper treatment with several immunomodulators to include IVIg can show remarkable improvement. We report an 11-year-old-girl diagnosed with anti-HMGCR myopathy with 6 years of follow-up.

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一名患有抗-HMGCR肌病的11岁女孩的六年随访。
抗-HMGCR肌病是一种免疫介导的坏死性肌病,其特征是亚急性、进行性近端肌无力和肌酸激酶(CK)水平升高。在儿科人群中,抗-HMGCR 肌病仅有少量病例报道,但十分罕见。虽然治疗方法尚未达成共识,但使用多种免疫调节剂(包括 IVIg)进行适当治疗后,病情会有显著改善。我们报告了一名被诊断患有抗-HMGCR 肌病的 11 岁女孩的病例,随访 6 年。
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CiteScore
7.20
自引率
4.30%
发文量
567
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