childhood-onset dystonia with optic atrophy and basal ganglia abnormalities

Summary
Synonym
  • DYSTONIA 29, CHILDHOOD-ONSET
  • DYTOABG
  • MECR-related neurologic disorder
  • MEPAN syndrome
  • Mitochondrial Enoyl CoA Reductase Protein-Associated Neurodegeneration
Definition
A dystonia that is characterized by characterized by onset of involuntary movements in the first decade of life and that has_material_basis_in homozygous or compound heterozygous mutation in the MECR gene on chromosome 1p35. Optic atrophy develops around the same time or slightly later.
Super Class
autosomal recessive disease dystonia
External Links
Disease Ontology
DOID:0081419
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
51102 MECR mitochondrial trans-2-enoyl-CoA reductase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024