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Results 1 - 9 of 9 for Demyelinating disease
  1. Charcot-Marie-Tooth disease 
    ... Rare Disorders (NORD) ClinicalTrials.gov CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A; CMT1A CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  2. SOX10 gene 
    ... similar disorder known as peripheral demyelinating neuropathy, central demyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease (PCWH). This rare condition is a variant of ...
    https://medlineplus.gov/genetics/gene/sox10 - Genetics
  3. Autosomal dominant leukodystrophy with autonomic disease 
    ... a second path to autosomal dominant adult-onset demyelinating leukodystrophy ... article on PubMed Central
    https://medlineplus.gov/...ant-leukodystrophy-with-autonomic-disease - Genetics
  4. MPZ gene 
    ... and molecular modelling of novel MPZ mutations in demyelinating and axonal ... in Charcot-Marie-Tooth disease. Neuromolecular Med. 2006;8(1-2):217-42. ...
    https://medlineplus.gov/genetics/gene/mpz - Genetics
  5. Yuan-Harel-Lupski syndrome 
    Yuan-Harel-Lupski (YUHAL) syndrome is a rare neurological condition that has a combination of features of two other disorders, Potocki-Lupski syndrome and ...
    https://medlineplus.gov/.../condition/yuan-harel-lupski-syndrome - Genetics
  6. TREM2 gene 
    ... profiles of dendritic cells of PLOSL patients link demyelinating CNS disorders ... complex result in an identical disease phenotype. Am J Hum Genet. 2002 Sep;71( ...
    https://medlineplus.gov/genetics/gene/trem2 - Genetics
  7. TYROBP gene 
    ... profiles of dendritic cells of PLOSL patients link demyelinating CNS disorders ... complex result in an identical disease phenotype. Am J Hum Genet. 2002 Sep;71( ...
    https://medlineplus.gov/genetics/gene/tyrobp - Genetics
  8. Guillain-Barré syndrome 
    ... type of Guillain-Barré syndrome is acute inflammatory demyelinating polyradiculoneuropathy ... regulation of the TNF gene: relevance to disease. J Leukoc Biol. 1999 Oct;66(4):562- ...
    https://medlineplus.gov/genetics/condition/guillain-barre-syndrome - Genetics
  9. LMNB1 gene 
    ... found to cause autosomal dominant leukodystrophy with autonomic disease (ADLD). This ... dominant adult-onset demyelinating leukodystrophy (ADLD). Hum Mol Genet. 2015 Jun 1; ...
    https://medlineplus.gov/genetics/gene/lmnb1 - Genetics