Aicardi-Goutières syndrome--observations of the Glasgow school

Eur J Paediatr Neurol. 2002:6 Suppl A:A67-70; discussion A37-9, A55-8, A65-6. doi: 10.1053/ejpn.2002.0578.
No abstract available

MeSH terms

  • Adolescent
  • Basal Ganglia Diseases / diagnosis
  • Basal Ganglia Diseases / genetics*
  • Basal Ganglia Diseases / pathology
  • Basement Membrane / pathology
  • Brain / pathology
  • Calcinosis / diagnosis
  • Calcinosis / genetics*
  • Calcinosis / pathology
  • Cerebrospinal Fluid / cytology
  • Chilblains / diagnosis
  • Chilblains / genetics
  • Chilblains / pathology
  • Child
  • Child, Preschool
  • Diagnostic Imaging
  • Disease Progression
  • Follow-Up Studies
  • Hereditary Central Nervous System Demyelinating Diseases / diagnosis
  • Hereditary Central Nervous System Demyelinating Diseases / genetics*
  • Hereditary Central Nervous System Demyelinating Diseases / pathology
  • Humans
  • Immunoglobulin M / analysis
  • Infant
  • Infant, Newborn
  • Interferon-alpha / cerebrospinal fluid*
  • Lymphocytosis / diagnosis
  • Lymphocytosis / genetics*
  • Lymphocytosis / pathology
  • Male
  • Microscopy, Fluorescence
  • Neurologic Examination
  • Skin / pathology
  • Syndrome

Substances

  • Immunoglobulin M
  • Interferon-alpha