Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: a new treatable disorder

Mov Disord. 2012 Sep 1;27(10):1317-22. doi: 10.1002/mds.25138. Epub 2012 Aug 23.

Abstract

Background: The first gene causing early-onset generalized dystonia with brain manganese accumulation has recently been identified. Mutations in the SLC30A10 gene, encoding a manganese transporter, cause a syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia.

Methods: We present 10-year longitudinal clinical features, MRI data, and treatment response to chelation therapy of the originally described patient with a proven homozygous mutation in SLC30A10.

Results: The patient presented with early-onset generalized dystonia and mild hyperbilirubinemia accompanied by elevated whole-blood manganese levels. T1-sequences in MRI showed hyperintensities in the basal ganglia and cerebellum, characteristic of manganese deposition. Treatment with intravenous disodium calcium edetate led to clinical improvement and reduction of hyperintensities in brain imaging.

Conclusions: We wish to highlight this rare disorder, which, together with Wilson's disease, is the only potentially treatable inherited metal storage disorder to date, that otherwise can be fatal as a result of complications of cirrhosis. © 2012 Movement Disorder Society.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain / metabolism*
  • Cation Transport Proteins / genetics*
  • Chelating Agents / therapeutic use
  • Dystonia / drug therapy
  • Dystonia / genetics*
  • Dystonia / pathology*
  • Female
  • Humans
  • Longitudinal Studies
  • Magnetic Resonance Imaging
  • Manganese / metabolism*
  • Mutation / genetics*
  • Pentetic Acid / therapeutic use
  • Young Adult
  • Zinc Transporter 8

Substances

  • Cation Transport Proteins
  • Chelating Agents
  • SLC30A8 protein, human
  • Zinc Transporter 8
  • Manganese
  • Pentetic Acid