| Literature DB >> 24836204 |
Kimihiko Kaneko1, Hiroshi Kuroda2, Rumiko Izumi1, Maki Tateyama1, Masaaki Kato1, Koichiro Sugimura3, Yasuhiko Sakata3, Yoshihiko Ikeda4, Ken-Ichi Hirano5, Masashi Aoki1.
Abstract
Mutations in PNPLA2 cause neutral lipid storage disease with myopathy (NLSDM) or triglyceride deposit cardiomyovasculopathy (TGCV). We report a 59-year-old patient with NLSDM/TGCV presenting marked asymmetric skeletal myopathy and cardiomyovasculopathy. Skeletal muscle and endomyocardial biopsies showed cytoplasmic vacuoles containing neutral lipid. Gene analysis revealed a novel homozygous mutation (c.576delC) in PNPLA2. We reviewed 37 genetically-proven NLSDM/TGCV cases; median age was 30 years; distribution of myopathy was proximal (69%) and distal predominant (16%); asymmetric myopathy (right>left) was reported in 41% of the patients. Frequently-affected muscles were posterior compartment of leg (75%), shoulder girdle to upper arm (50%), and paraspinal (33%). Skeletal muscle biopsies showed lipid accumulation in 100% and rimmed vacuoles in 22%. Frequent comorbidities were cardiomyopathy (44%), hyperlipidemia (23%), diabetes mellitus (24%), and pancreatitis (14%). PNPLA2 mutations concentrated in Exon 4-7 without apparent genotype-phenotype correlations. To know the characteristic features is essential for the early diagnosis of NLSDM/TGCV.Entities:
Keywords: Adipose triglyceride lipase; Asymmetric myopathy; Neutral lipid storage disease with myopathy; Patatin-like phospholipase domain-containing 2; Triglyceride deposit cardiomyovasculopathy
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Year: 2014 PMID: 24836204 DOI: 10.1016/j.nmd.2014.04.001
Source DB: PubMed Journal: Neuromuscul Disord ISSN: 0960-8966 Impact factor: 4.296