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  2. Leukodystrophy - Wikipedia

    en.wikipedia.org/wiki/Leukodystrophy

    Most of the research so far has been done on five types: (1) metachromatic leukodystrophy (MLD), (2) Krabbe disease, (3) X-Linked adrenoleukodystrophy (ALD), (4) Canavan disease, and (5) Alexander disease. Each type of leukodystrophy has a unique pathophysiology, but all five of these in some way affect a subset of glial cells, therefore ...

  3. 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.

  4. Hereditary diffuse leukoencephalopathy with spheroids

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

    Related disorders in the same disease spectrum as HDLS include Nasu-Hakola disease (polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy), and a type of leukodystrophy with pigment-filled macrophages called pigmentary orthochromatic leukodystrophy (POLD). [3] In addition to white matter disease, Nasu-Hakola causes bone ...

  5. Metachromatic leukodystrophy - Wikipedia

    en.wikipedia.org/wiki/Metachromatic_leukodystrophy

    Metachromatic leukodystrophy has an autosomal recessive pattern of inheritance. MLD has an autosomal recessive inheritance pattern. The inheritance probabilities per birth are as follows: [8] If both parents are carriers: 25% (1 in 4) of children will have the disease; 50% (2 in 4) of children will be carriers, but unaffected

  6. Leukoencephalopathy with vanishing white matter - Wikipedia

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

    Leukoencephalopathy with vanishing white matter (VWM disease) is an autosomal recessive neurological disease. The cause of the disease are mutations in any of the 5 genes encoding subunits of the translation initiation factor eIF2B: EIF2B1, EIF2B2, EIF2B3, EIF2B4, or EIF2B5. The disease belongs to a family of conditions called the Leukodystrophies.

  7. US approves first gene therapy for children with rare genetic ...

    www.aol.com/news/us-approves-first-gene-therapy...

    The one-time therapy, branded as Lenmeldy in the U.S., is approved for children in certain stages of disease progression, the Food and Drug Administration (FDA) said. US approves first gene ...

  8. Megalencephalic leukoencephalopathy with subcortical cysts

    en.wikipedia.org/wiki/Megalencephalic_leuko...

    The presence of frontal and temporal subcortical cysts is the main factor when diagnosing a patient with this disease. [11] In the late stages of the disease, patients have been noted to develop impaired coordination, overresponsive reflexes, and even seizures. MRI testing is used to study and diagnose patients with this disease.

  9. Progressive multifocal leukoencephalopathy - Wikipedia

    en.wikipedia.org/wiki/Progressive_multifocal_leu...

    Progressive multifocal leukoencephalopathy (PML) is a rare and often fatal viral disease characterized by progressive damage (-pathy) or inflammation of the white matter (leuko-) of the brain (-encephalo-) at multiple locations (multifocal). It is caused by the JC virus, which is normally present and kept under control by the immune system. The ...

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