Title : Severe steatohepatitis in a patient with a rare neutral lipid storage disorder due to ABHD5 mutation - Ronchetti_2008_J.Hepatol_49_474 |
Author(s) : Ronchetti A , Prati D , Pezzotta MG , Tavian D , Colombo R , Callea F , Colli A |
Ref : Journal of Hepatology , 49 :474 , 2008 |
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. |
PubMedSearch : Ronchetti_2008_J.Hepatol_49_474 |
PubMedID: 18644654 |
Gene_locus related to this paper: human-ABHD5 |
Mutation | S17fsX1_human-ABHD5 |
Gene_locus | human-ABHD5 |
Disease | Chanarin-Dorfman syndrome |
Ronchetti A, Prati D, Pezzotta MG, Tavian D, Colombo R, Callea F, Colli A (2008)
Severe steatohepatitis in a patient with a rare neutral lipid storage disorder due to ABHD5 mutation
Journal of Hepatology
49 :474
Ronchetti A, Prati D, Pezzotta MG, Tavian D, Colombo R, Callea F, Colli A (2008)
Journal of Hepatology
49 :474