Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 21 for Leukoencephalopathy with vanishing white matter 2
  1. Megalencephalic leukoencephalopathy with subcortical cysts 
    ... E, Estevez R. Expanding the spectrum of megalencephalic leukoencephalopathy with subcortical cysts in two patients with GLIALCAM mutations. Neurogenetics. 2014 Mar;15( ...
    https://medlineplus.gov/...eukoencephalopathy-with-subcortical-cysts - Genetics
  2. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy 
    ... cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL). Neuropathology. 2008 Apr;28(2):132-42. doi: 10.1111/j.1440-1789. ...
    https://medlineplus.gov/...cortical-infarcts-and-leukoencephalopathy - Genetics
  3. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 
    ... cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Stroke. 2007 Feb;38(2):276-80. doi: 10.1161/01.STR.0000254530. ...
    https://medlineplus.gov/...cortical-infarcts-and-leukoencephalopathy - Genetics
  4. Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia 
    ... factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids. Nat Genet. 2011 Dec 25;44(2):200-5. doi: 10.1038/ng.1027. Citation ...
    https://medlineplus.gov/...-with-axonal-spheroids-and-pigmented-glia - Genetics
  5. COL4A1-related brain small-vessel disease 
    ... C. COL4A1 mutation in Axenfeld-Rieger anomaly with leukoencephalopathy and stroke. Ann Neurol. 2007 Aug;62(2):177-84. doi: 10.1002/ana.21191. Citation ...
    https://medlineplus.gov/...col4a1-related-brain-small-vessel-disease - Genetics
  6. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation 
    ... and high lactate. Ann Neurol. 2003 Feb;53(2):252-8. doi: 10.1002/ana.10456. Citation on PubMed
    https://medlineplus.gov/...al-cord-involvement-and-lactate-elevation - Genetics
  7. TUBB4A-related leukodystrophy 
    ... the beta-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum. Am J Hum Genet. 2013 May 2;92(5):767-73. doi: 10.1016/j. ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  8. Alexander disease 
    ... Gorospe JR, Maletkovic J. Alexander disease and megalencephalic leukoencephalopathy with subcortical cysts: leukodystrophies arising from astrocyte dysfunction. Ment Retard Dev Disabil Res Rev. 2006;12(2):113-22. doi: 10.1002/mrdd.20101. No ...
    https://medlineplus.gov/genetics/condition/alexander-disease - Genetics
  9. CLCN2-related leukoencephalopathy 
    ... scientific literature. As its name suggests, CLCN2-related leukoencephalopathy is caused by mutations in the CLCN2 gene. The CLCN2 gene provides instructions for making a chloride channel called ClC-2. This channel transports negatively charged chlorine atoms (chloride ...
    https://medlineplus.gov/.../clcn2-related-leukoencephalopathy - Genetics
  10. Leukoencephalopathy with vanishing white matter 
    Leukoencephalopathy with vanishing white matter is a progressive disorder that mainly affects the brain and spinal cord (central nervous system). This disorder causes deterioration ...
    https://medlineplus.gov/...ncephalopathy-with-vanishing-white-matter - Genetics
previous · 1 · 2 · 3 · next