Hepatic Presentation of Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Case Report and Systematic Review.

MADD case report fatty liver hypertransaminasemia steatohepatitis

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2021
Historique:
received: 25 02 2021
accepted: 29 03 2021
entrez: 27 5 2021
pubmed: 28 5 2021
medline: 28 5 2021
Statut: epublish

Résumé

Diagnosis of pediatric steatohepatitis is a challenging issue due to a vast number of established and novel causes. Here, we report a child with Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) presenting with an underrated muscle weakness, exercise intolerance and an atypically severe steatotic liver involvement. A systematic literature review of liver involvement in MADD was performed as well. Our patient is a 11-year-old otherwise healthy, non-obese, male child admitted for some weakness/asthenia, vomiting and recurrent severe hypertransaminasemia (aspartate and alanine aminotransferases up to ×20 times upper limit of normal). Hepatic ultrasound showed a bright liver. MRI detected mild lipid storage of thighs muscles. A liver biopsy showed a micro-macrovacuolar steatohepatitis with minimal fibrosis. Main causes of hypertransaminasemia were ruled out. Serum aminoacids (increased proline), acylcarnitines (increased C4-C18) and a large excretion of urinary glutaric acid, ethylmalonic, butyric, isobutyric, 2-methyl-butyric and isovaleric acids suggested a diagnosis of MADD. Serum acylcarnitines and urinary organic acids fluctuated overtime paralleling serum transaminases during periods of illness/catabolic stress, confirming their recurrent nature. Genetic testing confirmed the diagnosis [homozygous c.1658A > G (p.Tyr553Cys) in exon 12 of the ETFDH gene]. Lipid-restricted diet and riboflavin treatment rapidly ameliorated symptoms, hepatic ultrasonography/enzymes, and metabolic profiles. Literature review (37 retrieved eligible studies, 283 patients) showed that liver is an extramuscular organ rarely involved in late-onset MADD (70 patients), and that amongst 45 patients who had fatty liver only nine had severe presentation.

Identifiants

pubmed: 34041209
doi: 10.3389/fped.2021.672004
pmc: PMC8143529
doi:

Types de publication

Case Reports

Langues

eng

Pagination

672004

Informations de copyright

Copyright © 2021 Siano, Mandato, Nazzaro, Iannicelli, Ciccarelli, Barretta, Mazzaccara, Ruoppolo, Frisso, Baldi, Tartaglione, Di Salle, Melis and Vajro.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Children (Basel). 2018 Dec 13;5(12):
pubmed: 30551665
J Hepatol. 2021 Apr;74(4):991-992
pubmed: 33493527
Mult Scler Relat Disord. 2021 Feb;48:102689
pubmed: 33383363
BMC Med Genomics. 2018 Apr 3;11(1):37
pubmed: 29615056
J Perinatol. 2000 Mar;20(2):120-8
pubmed: 10785889
J Neurol Sci. 2020 Apr 15;411:116707
pubmed: 32007756
Intern Med. 2011;50(21):2663-8
pubmed: 22041377
Brain Dev. 2016 Mar;38(3):293-301
pubmed: 26403312
J Neurol Neurosurg Psychiatry. 2010 Feb;81(2):231-6
pubmed: 19758981
Neuromuscul Disord. 2009 Mar;19(3):212-6
pubmed: 19249206
JIMD Rep. 2018;38:33-40
pubmed: 28456887
JIMD Rep. 2018;39:1-6
pubmed: 28685490
Respir Med Case Rep. 2015 May 11;15:92-4
pubmed: 26236614
Hum Mutat. 2003 Jul;22(1):12-23
pubmed: 12815589
Acta Myol. 2020 Mar 01;39(1):19-23
pubmed: 32607475
Zhongguo Dang Dai Er Ke Za Zhi. 2017 Oct;19(10):1104-1108
pubmed: 29046209
Mol Genet Metab. 2008 May;94(1):61-7
pubmed: 18289905
J Neurol Sci. 2015;353(1-2):84-6
pubmed: 25913573
Muscle Nerve. 2014 Mar;49(3):446-50
pubmed: 23893693
Pediatr Neurol. 2004 Sep;31(3):218-21
pubmed: 15351024
Genet Med. 2015 May;17(5):405-24
pubmed: 25741868
BMC Neurol. 2019 Dec 18;19(1):330
pubmed: 31852447
Mol Genet Metab Rep. 2018 Jun 11;16:15-19
pubmed: 29988809
Rev Neurol (Paris). 2016 Mar;172(3):231-41
pubmed: 27038534
Am J Phys Med Rehabil. 2020 Jun;99(6):e71-e74
pubmed: 31136308
J Hum Genet. 2014 May;59(5):256-61
pubmed: 24522293
Lipids Health Dis. 2018 Nov 13;17(1):254
pubmed: 30424791
Eur J Pediatr. 2013 May;172(5):707-10
pubmed: 23052622
Neurol Sci. 2016 Jul;37(7):1099-105
pubmed: 27000805
J Neurol Sci. 2011 Aug 15;307(1-2):166-7
pubmed: 21616504
J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S481-7
pubmed: 21088898
Internist (Berl). 2013 Aug;54(8):1016-22
pubmed: 23900454
World J Gastroenterol. 2013 May 14;19(18):2740-51
pubmed: 23687411
J Neurol Sci. 2018 Jan 15;384:121-125
pubmed: 29249369
J Child Neurol. 2010 Aug;25(8):954-60
pubmed: 20023066
World J Clin Cases. 2020 Mar 6;8(5):995-1001
pubmed: 32190638
Hum Mol Genet. 2013 Oct 1;22(19):3819-27
pubmed: 23727839
Am J Med Genet A. 2020 Oct;182(10):2426-2431
pubmed: 32804429
No To Hattatsu. 2000 Mar;32(2):163-8
pubmed: 10723193
J Inherit Metab Dis. 2014 May;37(3):399-404
pubmed: 24357026
Muscle Nerve. 2009 Mar;39(3):333-42
pubmed: 19208393
Front Pediatr. 2020 Mar 27;8:118
pubmed: 32292771
J Pediatr Gastroenterol Nutr. 2012 May;54(5):700-13
pubmed: 22395188
Orphanet J Rare Dis. 2014 Jul 22;9:117
pubmed: 25200064
Brain. 2007 Aug;130(Pt 8):2037-44
pubmed: 17412732
Clin Genet. 2010 Dec;78(6):565-9
pubmed: 20370797
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Apr;33(2):191-4
pubmed: 27060313

Auteurs

Maria Anna Siano (MA)

Postgraduate School of Pediatrics, Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Baronissi, Italy.

Claudia Mandato (C)

Unit of Pediatrics 1, AORN Santobono-Pausilipon, Naples, Italy.

Lucia Nazzaro (L)

Pediatric Clinic, AOU "S. Giovanni di Dio and Ruggi d'Aragona", Salerno, Italy.

Gennaro Iannicelli (G)

Pediatric Clinic, AOU "S. Giovanni di Dio and Ruggi d'Aragona", Salerno, Italy.

Gian Paolo Ciccarelli (GP)

Postgraduate School of Pediatrics, Faculty of Medicine University of Naples Federico II, Naples, Italy.

Ferdinando Barretta (F)

Department of Molecular Medicine and Medical Biotechnology, Faculty of Medicine University of Naples Federico II, Naples, Italy.
CEINGE-Biotecnologie Avanzate s.c.a r.l., Naples, Italy.

Cristina Mazzaccara (C)

Department of Molecular Medicine and Medical Biotechnology, Faculty of Medicine University of Naples Federico II, Naples, Italy.
CEINGE-Biotecnologie Avanzate s.c.a r.l., Naples, Italy.

Margherita Ruoppolo (M)

Department of Molecular Medicine and Medical Biotechnology, Faculty of Medicine University of Naples Federico II, Naples, Italy.
CEINGE-Biotecnologie Avanzate s.c.a r.l., Naples, Italy.

Giulia Frisso (G)

Department of Molecular Medicine and Medical Biotechnology, Faculty of Medicine University of Naples Federico II, Naples, Italy.
CEINGE-Biotecnologie Avanzate s.c.a r.l., Naples, Italy.

Carlo Baldi (C)

Pathology Unit, AOU "S. Giovanni di Dio and Ruggi d'Aragona", Salerno, Italy.

Salvatore Tartaglione (S)

Radiology Unit, AOU "S. Giovanni di Dio and Ruggi d'Aragona", Salerno, Italy.

Francesco Di Salle (F)

Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Baronissi, Italy.

Daniela Melis (D)

Postgraduate School of Pediatrics, Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Baronissi, Italy.
Pediatric Clinic, AOU "S. Giovanni di Dio and Ruggi d'Aragona", Salerno, Italy.

Pietro Vajro (P)

Postgraduate School of Pediatrics, Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Baronissi, Italy.
Pediatric Clinic, AOU "S. Giovanni di Dio and Ruggi d'Aragona", Salerno, Italy.
Postgraduate School of Pediatrics, Faculty of Medicine University of Naples Federico II, Naples, Italy.

Classifications MeSH