A novel disease-causing variant associated with a milder phenotype of AARS2-related leukodystrophy — A case report
Background and objectives: Adult-onset leukodystrophies are a rare group of neurological disorders characterized by progressive degeneration of the cerebral white matter. One of these diseases is caused by biallelic pathogenic variants in the AARS2 gene. We describe a patient with late-onset AARS2-r...
Saved in:
| Main Authors: | Joana Fernandes, João Moura, João Tarrio, Jorge Oliveira, Ana Lopes, João Parente Freixo, Gonçalo Videira |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-12-01
|
| Series: | Molecular Genetics and Metabolism Reports |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2214426924001101 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Atypical MEGDHEL Syndrome: A Milder Phenotype With Hepatic Presentation and Failure to Thrive Associated With a Homozygous Nonsense Variant of SERAC1
by: Rita Marchante Pita, et al.
Published: (2025-05-01) -
Overview of genetic variants in a cohort of Iranian patients with leukodystrophy
by: Mohadeseh Fathi, et al.
Published: (2025-07-01) -
Novel Gene Mutation Variant in Hypomyelinating Leukodystrophy-8: A Case Report
by: Shalesh Rohatgi, et al.
Published: (2024-11-01) -
Imaging of adult leukodystrophies
by: Claudia Costa Leite, et al.
Published: (2014-08-01) -
Recessive, pathogenic AARS1 variants display variable loss-of-function and dominant-negative effects
by: Molly E. Kuo, et al.
Published: (2025-06-01)