Literature DB >> 18644654

Severe steatohepatitis in a patient with a rare neutral lipid storage disorder due to ABHD5 mutation.

Anna Ronchetti1, Daniele Prati, Maria Grazia Pezzotta, Daniela Tavian, Roberto Colombo, Francesco Callea, Agostino Colli.   

Abstract

Fatty liver disease is mainly caused by alcohol consumption, excessive body weight, dyslipidemia and impaired glucose tolerance, but inherited disorders can sometimes be involved. We report the case of a 40-year-old woman with steatohepatitis and severe portal hypertension, associated with ichthyosis, cataract and hypoacusia. The clinical, pathological and genetic findings were consistent with a diagnosis of Chanarin-Dorfman syndrome (CDS), a rare autosomal recessive inherited neutral lipid storage disorder, and genetic analysis showed that a novel ABHD5 mutation is responsible.

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Year:  2008        PMID: 18644654     DOI: 10.1016/j.jhep.2008.05.027

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  12 in total

Review 1.  CGI-58: Versatile Regulator of Intracellular Lipid Droplet Homeostasis.

Authors:  Liqing Yu; Yi Li; Alison Grisé; Huan Wang
Journal:  Adv Exp Med Biol       Date:  2020       Impact factor: 2.622

Review 2.  Critical roles for α/β hydrolase domain 5 (ABHD5)/comparative gene identification-58 (CGI-58) at the lipid droplet interface and beyond.

Authors:  Amanda L Brown; J Mark Brown
Journal:  Biochim Biophys Acta Mol Cell Biol Lipids       Date:  2017-08-04       Impact factor: 4.698

3.  Dorfman-Chanarin Syndrome: A Rare Cause of Metabolic Associated Fatty Liver Disease Related to Homozygosity of the Nonsense Mutation c.934C>T (p.R312*).

Authors:  Rita Quelhas da Costa; Francisco Laranjeira; Isaura Duarte Ribeiro; António Filipe Santos; Filipe Nery
Journal:  GE Port J Gastroenterol       Date:  2021-07-07

4.  Deficiency of liver Comparative Gene Identification-58 causes steatohepatitis and fibrosis in mice.

Authors:  Feng Guo; Yinyan Ma; Anil K G Kadegowda; Jenna L Betters; Ping Xie; George Liu; Xiuli Liu; Hongming Miao; Juanjuan Ou; Xiong Su; Zhenlin Zheng; Bingzhong Xue; Hang Shi; Liqing Yu
Journal:  J Lipid Res       Date:  2013-06-03       Impact factor: 5.922

5.  Clinical and genetic characterization of Chanarin-Dorfman syndrome patients: first report of large deletions in the ABHD5 gene.

Authors:  Chiara Redaelli; Rosalind A Coleman; Laura Moro; Catherine Dacou-Voutetakis; Solaf Mohamed Elsayed; Daniele Prati; Agostino Colli; Donatella Mela; Roberto Colombo; Daniela Tavian
Journal:  Orphanet J Rare Dis       Date:  2010-12-01       Impact factor: 4.123

6.  Fat in the skin: Triacylglycerol metabolism in keratinocytes and its role in the development of neutral lipid storage disease.

Authors:  Franz Pw Radner; Susanne Grond; Guenter Haemmerle; Achim Lass; Rudolf Zechner
Journal:  Dermatoendocrinol       Date:  2011-04-01

7.  Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients.

Authors:  Elena Maria Pennisi; Marcello Arca; Enrico Bertini; Claudio Bruno; Denise Cassandrini; Adele D'amico; Matteo Garibaldi; Francesca Gragnani; Lorenzo Maggi; Roberto Massa; Sara Missaglia; Lucia Morandi; Olimpia Musumeci; Elena Pegoraro; Emanuele Rastelli; Filippo Maria Santorelli; Elisabetta Tasca; Daniela Tavian; Antonio Toscano; Corrado Angelini
Journal:  Orphanet J Rare Dis       Date:  2017-05-12       Impact factor: 4.123

Review 8.  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

9.  Early onset of Chanarin-Dorfman syndrome with severe liver involvement in a patient with a complex rearrangement of ABHD5 promoter.

Authors:  Sara Missaglia; Eugenia Ribeiro Valadares; Laura Moro; Eleonora Druve Tavares Faguntes; Raquel Quintão Roque; Bruno Giardina; Daniela Tavian
Journal:  BMC Med Genet       Date:  2014-03-14       Impact factor: 2.103

Review 10.  Omic studies reveal the pathogenic lipid droplet proteins in non-alcoholic fatty liver disease.

Authors:  Xuelin Zhang; Yang Wang; Pingsheng Liu
Journal:  Protein Cell       Date:  2016-10-18       Impact factor: 14.870

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