MYORG gene disease-causing variants in a family with primary familial brain calcification presenting with stroke-like episodes

Clin Genet. 2020 Nov;98(5):517-519. doi: 10.1111/cge.13836. Epub 2020 Sep 8.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Aged
  • Basal Ganglia Diseases / diagnosis
  • Basal Ganglia Diseases / diagnostic imaging
  • Basal Ganglia Diseases / genetics*
  • Basal Ganglia Diseases / pathology
  • Brain / diagnostic imaging*
  • Brain / pathology
  • Brain Diseases / diagnosis
  • Brain Diseases / diagnostic imaging
  • Brain Diseases / genetics*
  • Brain Diseases / pathology
  • Calcinosis / diagnosis
  • Calcinosis / diagnostic imaging
  • Calcinosis / genetics*
  • Calcinosis / pathology
  • Female
  • Glycoside Hydrolases / genetics*
  • Humans
  • Middle Aged
  • Mutation / genetics
  • Neurodegenerative Diseases / diagnosis
  • Neurodegenerative Diseases / diagnostic imaging
  • Neurodegenerative Diseases / genetics*
  • Neurodegenerative Diseases / pathology

Substances

  • Glycoside Hydrolases
  • MYORG protein, human

Supplementary concepts

  • Fahr's disease