
This review explores the clinical and pathological features, prognosis, and treatment of anti-HMGCR antibody positive immune-mediated necrotizing myopathy (HMGCR-IMNM). Recent findings highlight broader manifestations of the disease, including atypical presentations resembling limb-girdle muscular dystrophies and dermatomyositis-like skin conditions. Notably, clinicopathological symptoms are more common than previously recognized, emphasizing the need for comprehensive diagnostic approaches and tailored treatment strategies.
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