Ontology highlight
ABSTRACT: Objective
Acyl-CoA oxidase (ACOX1) deficiency is a rare disorder of peroxisomal very-long chain fatty acid oxidation. No reports detailing attempted treatment, longitudinal imaging, or neuropathology exist. We describe the natural history of clinical symptoms and brain imaging in two siblings with ACOX1 deficiency, including the younger sibling's response to allogeneic unrelated donor hematopoietic stem cell transplantation (HSCT).Methods
We conducted retrospective chart review to obtain clinical history, neuro-imaging, and neuropathology data. ACOX1 genotyping were performed to confirm the disease. In vitro fibroblast and neural stem cell fatty acid oxidation assays were also performed.Results
Both patients experienced a fatal neurodegenerative course, with late-st
SUBMITTER: Wang RY
PROVIDER: S-EPMC4332804 | biostudies-literature | 2014 Sep
REPOSITORIES: biostudies-literature