Leukoencephalopathy with neuroaxonal spheroids: Difference between revisions

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File:Neuron_with_oligodendrocyte_and_myelin_sheath-2.svg|Neuron with oligodendrocyte and myelin sheath
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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
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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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