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Biallelic SCO2 Variants Presenting as Motor-Predominant Axonal Neuropathy With Complex IV Deficiency
Adriana P Rebelo1, Katie Lutz2, Tiffany Grider3
1Dr. John T. Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Biallelic variants in SCO2, typically causing severe mitochondrial disease, can also present as a motor-predominant axonal neuropathy. This study confirms a loss-of-function mechanism for SCO2 variants in this rare presentation.
Area of Science:
- Genetics
- Mitochondrial Biology
- Neurology
Background:
- SCO2 is a mitochondrial copper chaperone essential for cytochrome c oxidase (COX) assembly.
- Mutations in SCO2 are classically linked to severe multisystem mitochondrial disorders.
- A motor-predominant axonal neuropathy phenotype associated with SCO2 variants is rarely reported.
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