[Congenital cerebral hypomyelination---Pelizaeus-Merzbacher disease and associated disorders]

No To Hattatsu. 2011 Nov;43(6):435-42.
[Article in Japanese]

Abstract

Congenital cerebral hypomyelination includes a group of genetic disorders, such as Pelizaeus-Merzbacher disease (PMD), and is characterized by hypomyelination of the cerebral white matter. Until recently, no classification system was available for congenital hypomyelination disorders that are clinically and genetically excluded for PMD. However, the establishment of new disease entities with gene discoveries has generated a clinical need for a new classification and diagnostic criteria for this group of disorders. Here, we review the recent findings on congenital cerebral hypomyelination, which includes 11 diseases, with a novel disease classification and diagnostic criteria with flow charts.

Publication types

  • Review

MeSH terms

  • Chaperonin 60 / genetics
  • Charcot-Marie-Tooth Disease* / classification
  • Charcot-Marie-Tooth Disease* / diagnosis
  • Charcot-Marie-Tooth Disease* / genetics
  • Chromosomes, Human, Pair 18 / genetics
  • Connexins / genetics
  • Diagnosis, Differential
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Magnetic Resonance Imaging
  • Membrane Proteins / genetics
  • Mitochondrial Proteins / genetics
  • Monocarboxylic Acid Transporters / genetics
  • Mutation*
  • Myelin Proteolipid Protein / genetics*
  • Pathology, Molecular*
  • Pelizaeus-Merzbacher Disease* / classification
  • Pelizaeus-Merzbacher Disease* / diagnosis
  • Pelizaeus-Merzbacher Disease* / genetics
  • SOXE Transcription Factors / genetics
  • Symporters

Substances

  • Chaperonin 60
  • Connexins
  • FAM126A protein, human
  • HSPD1 protein, human
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Mitochondrial Proteins
  • Monocarboxylic Acid Transporters
  • Myelin Proteolipid Protein
  • PLP1 protein, human
  • SLC16A2 protein, human
  • SOX10 protein, human
  • SOXE Transcription Factors
  • Symporters
  • connexin 47

Supplementary concepts

  • Charcot-Marie-Tooth disease, Type 4E