Literature DB >> 22964912

A novel mutation in PNPLA2 leading to neutral lipid storage disease with myopathy.

Daniel B Ash1, Dimitra Papadimitriou, Arthur P Hays, Salvatore Dimauro, Michio Hirano.   

Abstract

BACKGROUND: Mutations in PNPLA2, a gene encoding adipose triglyceride lipase, lead to neutral lipid storage disease with myopathy.
OBJECTIVE: To report the clinical and molecular features of a case of neutral lipid storage disease with myopathy resulting from a novel mutation in PNPLA2.
DESIGN: Case report.
SETTING: University hospital. PATIENT: A 65-year-old man with progressive muscle weakness and high serum creatine kinase levels. INTERVENTION: Direct sequencing of the PNPLA2 gene.
RESULTS: Identification of a novel homozygous mutation in the patient's PNPLA2 gene confirmed the suspected diagnosis of neutral lipid storage disease with myopathy.
CONCLUSION: Screening of the PNPLA2 gene should be considered for patients presenting with high levels of creatine kinase, progressive muscle weakness, and systemic lipid accumulation. The presence of Jordans anomaly can be a strong diagnostic clue.

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Year:  2012        PMID: 22964912      PMCID: PMC4961086          DOI: 10.1001/archneurol.2011.2600

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  12 in total

1.  Neutral-lipid storage disease: a new disorder of lipid metabolism.

Authors:  I Chanarin; A Patel; G Slavin; E J Wills; T M Andrews; G Stewart
Journal:  Br Med J       Date:  1975-03-08

2.  The familial occurrence of fat containing vacuoles in the leukocytes diagnosed in two brothers suffering from dystrophia musculorum progressiva (ERB.).

Authors:  G H JORDANS
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3.  Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 gene.

Authors:  Hasan O Akman; Guido Davidzon; Kurenai Tanji; Emma J Macdermott; Louann Larsen; Mercy M Davidson; Ronald G Haller; Lidia S Szczepaniak; Thomas J A Lehman; Michio Hirano; Salvatore DiMauro
Journal:  Neuromuscul Disord       Date:  2010-05-14       Impact factor: 4.296

4.  Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome.

Authors:  C Lefèvre; F Jobard; F Caux; B Bouadjar; A Karaduman; R Heilig; H Lakhdar; A Wollenberg; J L Verret; J Weissenbach; M Ozgüc; M Lathrop; J F Prud'homme; J Fischer
Journal:  Am J Hum Genet       Date:  2001-10-02       Impact factor: 11.025

5.  The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy.

Authors:  Judith Fischer; Caroline Lefèvre; Eva Morava; Jean-Marie Mussini; Pascal Laforêt; Anne Negre-Salvayre; Mark Lathrop; Robert Salvayre
Journal:  Nat Genet       Date:  2006-12-24       Impact factor: 38.330

6.  Brummer lipase is an evolutionary conserved fat storage regulator in Drosophila.

Authors:  Sebastian Grönke; Alexander Mildner; Sonja Fellert; Norbert Tennagels; Stefan Petry; Günter Müller; Herbert Jäckle; Ronald P Kühnlein
Journal:  Cell Metab       Date:  2005-05       Impact factor: 27.287

7.  Fat mobilization in adipose tissue is promoted by adipose triglyceride lipase.

Authors:  Robert Zimmermann; Juliane G Strauss; Guenter Haemmerle; Gabriele Schoiswohl; Ruth Birner-Gruenberger; Monika Riederer; Achim Lass; Georg Neuberger; Frank Eisenhaber; Albin Hermetter; Rudolf Zechner
Journal:  Science       Date:  2004-11-19       Impact factor: 47.728

8.  Characterization of desnutrin functional domains: critical residues for triacylglycerol hydrolysis in cultured cells.

Authors:  Robin E Duncan; Yuhui Wang; Maryam Ahmadian; Jennifer Lu; Eszter Sarkadi-Nagy; Hei Sook Sul
Journal:  J Lipid Res       Date:  2009-08-19       Impact factor: 5.922

9.  The C-terminal region of human adipose triglyceride lipase affects enzyme activity and lipid droplet binding.

Authors:  Martina Schweiger; Gabriele Schoiswohl; Achim Lass; Franz P W Radner; Guenter Haemmerle; Roland Malli; Wolfgang Graier; Irina Cornaciu; Monika Oberer; Robert Salvayre; Judith Fischer; Rudolf Zechner; Robert Zimmermann
Journal:  J Biol Chem       Date:  2008-04-29       Impact factor: 5.157

10.  Coatomer-dependent protein delivery to lipid droplets.

Authors:  Krishnakant G Soni; Gonzalo A Mardones; Rachid Sougrat; Elena Smirnova; Catherine L Jackson; Juan S Bonifacino
Journal:  J Cell Sci       Date:  2009-06-01       Impact factor: 5.285

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  4 in total

1.  Neutral lipid storage disease with myopathy presenting asymmetrical muscle weakness: a case report.

Authors:  Jinru Zhang; Jingzhe Han; Yaye Wang; Yue Wu; Xueqin Song; Guang Ji
Journal:  Int J Clin Exp Pathol       Date:  2020-03-01

2.  Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvement.

Authors:  Sara Missaglia; Lorenzo Maggi; Marina Mora; Sara Gibertini; Flavia Blasevich; Piergiuseppe Agostoni; Laura Moro; Denise Cassandrini; Filippo Maria Santorelli; Simonetta Gerevini; Daniela Tavian
Journal:  Neuromuscul Disord       Date:  2017-01-17       Impact factor: 4.296

Review 3.  Neutral Lipid Storage Diseases as Cellular Model to Study Lipid Droplet Function.

Authors:  Sara Missaglia; Rosalind A Coleman; Alvaro Mordente; Daniela Tavian
Journal:  Cells       Date:  2019-02-21       Impact factor: 6.600

Review 4.  Of mice and men: The physiological role of adipose triglyceride lipase (ATGL).

Authors:  Renate Schreiber; Hao Xie; Martina Schweiger
Journal:  Biochim Biophys Acta Mol Cell Biol Lipids       Date:  2018-10-25       Impact factor: 4.698

  4 in total

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