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Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review.

Authors :
Chavany J
Cano A
Roquelaure B
Bourgeois P
Boubnova J
Gaignard P
Hoebeke C
Reynaud R
Rhomer B
Slama A
Badens C
Chabrol B
Fabre A
Source :
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie [Arch Pediatr] 2020 Apr; Vol. 27 (3), pp. 155-159. Date of Electronic Publication: 2020 Mar 04.
Publication Year :
2020

Abstract

Acute liver failure (ALF) in childhood is a life-threatening emergency. ALF is often caused by drug toxicity, autoimmune hepatitis, inherited metabolic diseases, and infections. However, despite thorough investigations, a cause cannot be determined in approximately 50% of cases. Here, we report three cases with recurrent ALF caused by NBAS and SCYL1 pathogenic variants. These patients did not present with any other phenotypic sign usually associated with NBAS and SCYL1 pathogenic variants. Two of them underwent liver transplantation and are healthy without recurrence of ALF. We propose NBAS and SCYL1 genetic analysis in children with unexplained fever-triggered recurrent ALF even without a typical phenotype.<br /> (Copyright © 2020 French Society of Pediatrics. Published by Elsevier Masson SAS. All rights reserved.)

Details

Language :
English
ISSN :
1769-664X
Volume :
27
Issue :
3
Database :
MEDLINE
Journal :
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Publication Type :
Academic Journal
Accession number :
32146038
Full Text :
https://doi.org/10.1016/j.arcped.2020.01.003