Literature DB >> 32009609

Inborn errors of metabolism in the differential diagnosis of fatty liver disease.

Yılmaz Yıldız1, Hatice Serap Sivri2.   

Abstract

Nonalcoholic fatty liver disease (NAFLD) has become the most common chronic liver disease across all age groups. Obesity, diabetes, and metabolic syndrome, are the primary causes that are closely linked with the development of NAFLD. However, in young children, rare inborn errors of metabolism are predominant secondary causes of NAFLD. Furthermore, inborn errors of metabolism causing hepatosteatosis are often misdiagnosed as NAFLD in adolescents and adults. Many inborn errors of metabolism are treatable disorders and therefore require special consideration. This review aims to summarize the basic characteristics and diagnostic clues of inborn errors of metabolism associated with fatty liver disease. A suggested clinical and laboratory diagnostic approach is also discussed.

Entities:  

Year:  2020        PMID: 32009609      PMCID: PMC7075690          DOI: 10.5152/tjg.2019.19367

Source DB:  PubMed          Journal:  Turk J Gastroenterol        ISSN: 1300-4948            Impact factor:   1.852


  67 in total

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4.  Inherent lipid metabolic dysfunction in glycogen storage disease IIIa.

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Journal:  Biochem Biophys Res Commun       Date:  2014-12-05       Impact factor: 3.575

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Review 6.  Gastrointestinal and hepatic manifestations of mitochondrial disorders.

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Journal:  J Inherit Metab Dis       Date:  2013-05-15       Impact factor: 4.982

7.  Dihydrolipoamide dehydrogenase deficiency: a still overlooked cause of recurrent acute liver failure and Reye-like syndrome.

Authors:  Anaïs Brassier; Chris Ottolenghi; Audrey Boutron; Anne-Marie Bertrand; Séverine Valmary-Degano; Jean-Paul Cervoni; Dominique Chrétien; Jean-Baptiste Arnoux; Laurence Hubert; Daniel Rabier; Florence Lacaille; Yves de Keyzer; Vincent Di Martino; Pascale de Lonlay
Journal:  Mol Genet Metab       Date:  2013-02-01       Impact factor: 4.797

Review 8.  Carnitine transport and fatty acid oxidation.

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Journal:  Biochim Biophys Acta       Date:  2016-01-29

9.  Clinical Features of Lysosomal Acid Lipase Deficiency.

Authors:  Barbara K Burton; Patrick B Deegan; Gregory M Enns; Ornella Guardamagna; Simon Horslen; Gerard K Hovingh; Steve J Lobritto; Vera Malinova; Valerie A McLin; Julian Raiman; Maja Di Rocco; Saikat Santra; Reena Sharma; Jolanta Sykut-Cegielska; Chester B Whitley; Stephen Eckert; Vassili Valayannopoulos; Anthony G Quinn
Journal:  J Pediatr Gastroenterol Nutr       Date:  2015-12       Impact factor: 2.839

10.  Aminoacyl-tRNA synthetase deficiencies in search of common themes.

Authors:  Imre F Schene; Gautam Kok; Sabine A Fuchs; Jurriaan M Jansen; Peter G J Nikkels; Koen L I van Gassen; Suzanne W J Terheggen-Lagro; Saskia N van der Crabben; Sanne E Hoeks; Laetitia E M Niers; Nicole I Wolf; Maaike C de Vries; David A Koolen; Roderick H J Houwen; Margot F Mulder; Peter M van Hasselt
Journal:  Genet Med       Date:  2018-06-06       Impact factor: 8.822

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  3 in total

1.  Atypical Reye syndrome: three cases of a problem that pediatricians should consider and remember.

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Journal:  Acta Biomed       Date:  2021-04-30

Review 2.  Benefits of Physical Exercise as Approach to Prevention and Reversion of Non-Alcoholic Fatty Liver Disease in Children and Adolescents with Obesity.

Authors:  Valeria Calcaterra; Vittoria Carlotta Magenes; Matteo Vandoni; Clarissa Berardo; Luca Marin; Alice Bianchi; Erika Cordaro; Giustino Simone Silvestro; Dario Silvestri; Vittoria Carnevale Pellino; Cristina Cereda; Gianvincenzo Zuccotti
Journal:  Children (Basel)       Date:  2022-08-05

Review 3.  Metabolic-associated fatty liver disease from childhood to adulthood: State of art and future directions.

Authors:  Francesca Lanzaro; Stefano Guarino; Elisabetta D'Addio; Alessandra Salvatori; Josè Alberto D'Anna; Pierluigi Marzuillo; Emanuele Miraglia Del Giudice; Anna Di Sessa
Journal:  World J Hepatol       Date:  2022-06-27
  3 in total

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