Pediatric Anti-HMGCR Myopathy–A Case Report

Anti -HMGCR (3-hydroxy -3-Methyl glutaryl -Coenzyme A reductase) autoantibody positive Immune -mediated necrotizing myopathy was 1st recognized in an adult patient with a history of statin exposure.The clinico pathologic spectrum of the disease is constantly updated, including in statin unexposed patients, childhood-onset Cases in pediatric and adult patient with a LGMD phenotype.HMGCR myopathy should be considered as a differential diagnosis in children with idiopathic limb girdle muscular dystrophy with silent neuromuscular family history.In 2017 at least four reports described further cases of pediatric anti-HMGCR associated necrotizing myopathies [1].

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Publication Details

Journal
Journal of Orthopedics & Rheumatology
Published
2025-01-01
DOI
https://doi.org/10.13188/2334-2846.1000061
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
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article

Pediatric Anti-HMGCR Myopathy–A Case Report

Ajay Gupta
Journal of Orthopedics & Rheumatology
Inflammatory Myopathies and Dermatomyositis
article

Pediatric Anti-HMGCR Myopathy–A Case Report

Ajay Gupta
article en

Abstract

Anti -HMGCR (3-hydroxy -3-Methyl glutaryl -Coenzyme A reductase) autoantibody positive Immune -mediated necrotizing myopathy was 1st recognized in an adult patient with a history of statin exposure.The clinico pathologic spectrum of the disease is constantly updated, including in statin unexposed patients, childhood-onset Cases in pediatric and adult patient with a LGMD phenotype.HMGCR myopathy should be considered as a differential diagnosis in children with idiopathic limb girdle muscular dystrophy with silent neuromuscular family history.In 2017 at least four reports described further cases of pediatric anti-HMGCR associated necrotizing myopathies [1].

Journal of Orthopedics & RheumatologyVol. 11(1)
CSIR National Physical Laboratory of India (IN)
Gender equality
Openalex Percentile: Top 80%
Inflammatory Myopathies and Dermatomyositis
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