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  2. Leukoencephalopathy with vanishing white matter - Wikipedia

    en.wikipedia.org/wiki/Leukoencephalopathy_with...

    The neurological disorders and symptoms which occur with VWM are not specific to countries; they are the same all over the world. [4] Neurological abnormalities may not always be present in those who experience onset as adults. Symptoms generally appear in young children or infants who were previously developing fairly normally. [citation needed]

  3. Leukodystrophy - Wikipedia

    en.wikipedia.org/wiki/Leukodystrophy

    The degeneration of white matter can be seen in an MRI scan and is used to diagnose leukodystrophy. Leukodystrophy is characterized by specific symptoms, including decreased motor function, muscle rigidity, and eventual degeneration of sight and hearing. While the disease is fatal, the age of onset is a key factor, as infants have a typical ...

  4. Binswanger's disease - Wikipedia

    en.wikipedia.org/wiki/Binswanger's_disease

    Binswanger's disease, also known as subcortical leukoencephalopathy and subcortical arteriosclerotic encephalopathy, [1] is a form of small-vessel vascular dementia caused by damage to the white brain matter. [2] White matter atrophy can be caused by many circumstances including chronic hypertension as well as old age. [3]

  5. Leukoencephalopathy - Wikipedia

    en.wikipedia.org/wiki/Leukoencephalopathy

    Leukoencephalopathy (leukodystrophy-like diseases) is a term that describes all of the brain white matter diseases, whether their molecular cause is known or unknown. [1] It can refer specifically to any of these diseases: Progressive multifocal leukoencephalopathy; Toxic leukoencephalopathy

  6. Leukoencephalopathy with neuroaxonal spheroids - Wikipedia

    en.wikipedia.org/wiki/Leukoencephalopathy_with_n...

    Leukoencephalopathy with neuroaxonal spheroids (LENAS), also known as adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP), hereditary diffuse leukoencephalopathy with spheroids (HDLS) and pigmentary orthochromatic leukodystrophy (POLD) [1] is an extremely rare kind of leukoencephalopathy and is classified as a neurodegenerative disease.

  7. Toxic leukoencephalopathy - Wikipedia

    en.wikipedia.org/wiki/Toxic_leukoencephalopathy

    Toxic leukoencephalopathy is a rare condition that is characterized by progressive damage (-pathy) to white matter (-leuko-) in the brain (-encephalo-), particularly myelin, due to causes such as exposure to substance use, environmental toxins, or chemotherapeutic drugs. The prevalence of this disease is infrequent and often goes unreported ...

  8. Hereditary diffuse leukoencephalopathy with spheroids

    en.wikipedia.org/wiki/Hereditary_diffuse_leuko...

    HDLS falls under the category of brain white matter diseases called leukoencephalopathies that are characterized by some degree of white matter dysfunction. HDLS has white matter lesions with abnormalities in myelin sheath around axons, where the causative influences are being continually explored based upon recent genetic findings. Studies by ...

  9. Encephalomalacia - Wikipedia

    en.wikipedia.org/wiki/Encephalomalacia

    White softening is another form of cerebral softening. This type of softening occurs in areas that continue to be poorly perfused, with little to no blood flow. These are known as "pale" or "anemic infarcts" and are areas that contain dead neuronal tissue , which result in a softening of the cerebrum.

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