Unusual pure motor axonal neuropathy in a Burmese family with galactosialidosis

J Inherit Metab Dis. 1998 Dec;21(8):869-70. doi: 10.1023/a:1005431021025.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Female
  • Fibroblasts / enzymology
  • Humans
  • Leukocytes / enzymology
  • Lysosomal Storage Diseases / complications*
  • Lysosomal Storage Diseases / diagnosis
  • Male
  • Motor Neuron Disease / etiology*
  • Myanmar
  • Neuraminidase / deficiency*
  • beta-Galactosidase / deficiency*

Substances

  • Neuraminidase
  • beta-Galactosidase