MRI in LARS1 deficiency-Spectrum, patterns, and correlation with acute neurological deterioration.

ILFS1 LARS1 MRI acute liver failure aminoacyl‐tRNA synthetase deficiencies cerebellar watershed encephalopathy metabolic stroke thalamus

Journal

Journal of inherited metabolic disease
ISSN: 1573-2665
Titre abrégé: J Inherit Metab Dis
Pays: United States
ID NLM: 7910918

Informations de publication

Date de publication:
01 Jul 2024
Historique:
revised: 10 05 2024
received: 28 03 2024
accepted: 14 05 2024
medline: 2 7 2024
pubmed: 2 7 2024
entrez: 2 7 2024
Statut: aheadofprint

Résumé

Leucine aminoacyl tRNA-synthetase 1 (LARS1)-deficiency (infantile liver failure syndrome type 1 (ILFS1)) has a multisystemic phenotype including fever-associated acute liver failure (ALF), chronic neurologic abnormalities, and encephalopathic episodes. In order to better characterize encephalopathic episodes and MRI changes, 35 cranial MRIs from 13 individuals with LARS1 deficiency were systematically assessed and neurological phenotype was analyzed. All individuals had developmental delay and 10/13 had seizures. Encephalopathic episodes in 8/13 were typically associated with infections, presented with seizures and reduced consciousness, mostly accompanied by hepatic dysfunction, and recovery in 17/19 episodes. Encephalopathy without hepatic dysfunction occurred in one individual after liver transplantation. On MRI, 5/7 individuals with MRI during acute encephalopathy had deep gray matter and brainstem changes. Supratentorial cortex involvement (6/13) and cerebellar watershed injury (4/13) occurred with seizures and/or encephalopathy. Abnormal brainstem contour on sagittal images (8/13), atrophy (8/13), and myelination delay (8/13) were not clearly associated with encephalopathy. The pattern of deep gray matter and brainstem changes are apparently characteristic of encephalopathy in LARS1-deficiency, differing from patterns of hepatic encephalopathy or metabolic stroke in organic acidurias and mitochondrial diseases. While the pathomechanism remains unclear, fever and energy deficit during infections might be causative; thus, sufficient glucose and protein intake along with pro-active fever management is suggested. As severe episodes were observed during influenza infections, we strongly recommend seasonal vaccination.

Identifiants

pubmed: 38951950
doi: 10.1002/jimd.12764
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Deutsche Leberstiftung
ID : S163/10052/2018

Informations de copyright

© 2024 SSIEM.

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Auteurs

Nicole Hammann (N)

Medical Faculty, University Hospital Heidelberg, Center for Child and Adolescent Medicine, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.

Dominic Lenz (D)

Medical Faculty, University Hospital Heidelberg, Center for Child and Adolescent Medicine, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.

Alyssa Bianzano (A)

Medical Faculty, University Hospital Heidelberg, Center for Child and Adolescent Medicine, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.

Ralf A Husain (RA)

Centre for Inborn Metabolic Disorders, Department of Neuropediatrics, Jena University Hospital, Jena, Germany.

Eva Forman (E)

National Centre for Inherited Metabolic Disorders, Children's Health Ireland at Temple Street and Crumlin, Dublin, Ireland.

Jonathan A Bernstein (JA)

Department of Pediatrics, Stanford School of Medicine, Stanford, California, USA.
Center for Undiagnosed Diseases, Stanford University, Stanford, California, USA.

Tal Dattner (T)

Medical Faculty, University Hospital Heidelberg, Center for Child and Adolescent Medicine, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.

Marc Engelen (M)

Department of Child Neurology, Amsterdam Leukodystrophy Center, Emma Children's Hospital, Amsterdam UMC Location, University of Amsterdam, Amsterdam Neuroscience, Amsterdam, The Netherlands.

Andrea K Hanson-Kahn (AK)

Department of Genetics, Stanford University School of Medicine, Palo Alto, California, USA.
Department of Pediatrics, Division of Medical Genetics, Lucile Packard Children's Hospital, Palo Alto, California, USA.

Bertrand Isidor (B)

CHU Nantes, Service de Génétique Médicale, Nantes, France.
INSERM, CNRS, UNIV Nantes, l'institut du thorax, Nantes, France.

Urania Kotzaeridou (U)

Medical Faculty, University Hospital Heidelberg, Center for Child and Adolescent Medicine, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.

Anna Tietze (A)

Institute of Neuroradiology, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Regina Trollmann (R)

Department of Neuropaediatrics, University Hospital Erlangen, Erlangen, Germany.

Claudia Weiß (C)

Department of Neuropediatrics, Sozialpädiatrisches Zentrum (SPZ), Center for Chronically Sick Children, Charité-Universitätsmedizin, Berlin, Germany.
Humboldt-Universität zu Berlin, Berlin Institute of Health, Berlin, Germany.

Bruce H R Wolffenbuttel (BHR)

Department of Endocrinology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Stefan Kölker (S)

Medical Faculty, University Hospital Heidelberg, Center for Child and Adolescent Medicine, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.

Georg F Hoffmann (GF)

Medical Faculty, University Hospital Heidelberg, Center for Child and Adolescent Medicine, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.

Ellen Crushell (E)

National Centre for Inherited Metabolic Disorders, Children's Health Ireland at Temple Street and Crumlin, Dublin, Ireland.

Christian Staufner (C)

Medical Faculty, University Hospital Heidelberg, Center for Child and Adolescent Medicine, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.

Alexander Mohr (A)

Department of Neuroradiology, University Hospital Heidelberg, Heidelberg, Germany.

Inga Harting (I)

Department of Neuroradiology, University Hospital Heidelberg, Heidelberg, Germany.

Classifications MeSH