Leukoencephalopathy with neuroaxonal spheroids: Difference between revisions

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<gallery>
File:Neuron_with_oligodendrocyte_and_myelin_sheath-2.svg|Neuron with oligodendrocyte and myelin sheath
File:Missense_Mutation_Example.jpg|Missense mutation example
File:Lobes_of_the_brain.jpg|Lobes of the brain
File:1511_The_Limbic_Lobe.jpg|The limbic lobe
File:White_Matter_Lesions_(48601156232).jpg|White matter lesions
File:Blausen_0617_LumbarPuncture.png|Lumbar puncture
File:Stem_cell_differentiation.svg|Stem cell differentiation
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Latest revision as of 11:47, 18 February 2025

Leukoencephalopathy with neuroaxonal spheroids
Synonyms
Pronounce
Field neurology
Symptoms
Complications
Onset
Duration
Types
Causes
Risks
Diagnosis
Differential diagnosis
Prevention
Treatment
Medication
Prognosis
Frequency
Deaths


Leukoencephalopathy with neuroaxonal spheroids is a special kind of leukoencephalopathy. It is a cause of severe and subacute dementia. It is inherited, following an autosomal dominant pattern.

It usually presents in childhood but it can also have an adult onset,<ref>,

 Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP): Integrating the literature on hereditary diffuse leukoencephalopathy with spheroids (HDLS) and pigmentary orthochromatic leukodystrophy (POLD), 
 Journal of Clinical Neuroscience, 
 
 Vol. 48(Issue: 1),
 pp. 42–49,
 DOI: 10.1016/j.jocn.2017.10.060,
 PMID: 29122458,</ref> in which case it can present MRIs that mimic those of progressive multiple sclerosis.<ref>, 
 Sporadic adult-onset leukoencephalopathy with neuroaxonal spheroids mimicking cerebral MS, 
 Neurology, 
 
 Vol. 70(Issue: 13 Pt 2),
 pp. 1128–33,
 DOI: 10.1212/01.wnl.0000304045.99153.8f,
 PMID: 18287567,</ref>

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