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There is a page named "Leukodystrophy" on Wikipedia

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  • Thumbnail for Leukodystrophy
    Leukodystrophies are a group of, usually, inherited disorders, characterized by degeneration of the white matter in the brain. The word leukodystrophy...
    35 KB (3,848 words) - 09:25, 19 February 2025
  • Metachromatic leukodystrophy (MLD) is a lysosomal storage disease which is commonly listed in the family of leukodystrophies as well as among the sphingolipidoses...
    29 KB (3,400 words) - 16:21, 17 February 2025
  • Thumbnail for Leukoencephalopathy with vanishing white matter
    or EIF2B5. The disease belongs to a family of conditions called the Leukodystrophies.[citation needed] Onset usually occurs in childhood, however some adult...
    20 KB (2,511 words) - 20:58, 7 November 2023
  • Thumbnail for Krabbe disease
    Krabbe disease (KD) (also known as globoid cell leukodystrophy or galactosylceramide lipidosis) is a rare and often fatal lysosomal storage disease that...
    23 KB (2,314 words) - 08:41, 26 February 2025
  • aminoacylase 2, and is one of a group of genetic diseases referred to as leukodystrophies. It is characterized by degeneration of myelin in the phospholipid...
    18 KB (1,924 words) - 20:21, 13 February 2025
  • Thumbnail for Alexander disease
    Alexander disease is a very rare autosomal dominant leukodystrophy, which are neurological conditions caused by anomalies in the myelin which protects...
    14 KB (1,455 words) - 19:52, 23 August 2024
  • Thumbnail for Leukoencephalopathy
    Leukoencephalopathy (leukodystrophy-like diseases) is a term that describes all of the brain white matter diseases, whether their molecular cause is known...
    2 KB (231 words) - 09:31, 7 November 2024
  • CNS demyelinating disease. It belongs to a group of disorders called leukodystrophies. It is characterized by early-onset enlargement of the head (macrocephaly)...
    13 KB (1,370 words) - 23:18, 9 February 2025
  • Thumbnail for Pelizaeus–Merzbacher disease
    (hypomyelination) and belongs to a group of genetic diseases referred to as leukodystrophies. The hallmark signs and symptoms of Pelizaeus–Merzbacher disease include...
    13 KB (1,188 words) - 16:15, 17 November 2024
  • angiitis Leukodystrophy reunion type Leukodystrophy, globoid cell Leukodystrophy, metachromatic Leukodystrophy, pseudometachromatic Leukodystrophy, Sudanophilic...
    10 KB (900 words) - 15:15, 1 April 2022
  • Thumbnail for Autosomal dominant leukodystrophy with autonomic disease
    Autosomal dominant leukodystrophy with autonomic disease is a rare neurological condition of genetic origin which is characterized by gradual demyelination...
    19 KB (1,803 words) - 19:55, 21 January 2025
  • Thumbnail for Lysosomal storage disease
    gangliosidoses, including Gaucher's and Niemann–Pick diseases (E75.2-E75.3) Leukodystrophies (E76.0) Mucopolysaccharidoses, including Hunter syndrome and Hurler...
    18 KB (1,829 words) - 10:05, 14 December 2024
  • Libmeldy among others, is a gene therapy treatment for metachromatic leukodystrophy developed by Orchard Therapeutics. It contains an autologous CD34⁺ cell...
    14 KB (1,032 words) - 06:17, 6 October 2024
  • Thumbnail for Arylsulfatase A
    gene. A deficiency in Arylsulfatase A is associated with metachromatic leukodystrophy, an autosomal recessive disease. Multiple sulfatase deficiency (MSD)...
    9 KB (958 words) - 17:13, 9 September 2024
  • Thumbnail for Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
    RVCL-S, also previously known as retinal vasculopathy with cerebral leukodystrophy, RVCL; or cerebroretinal vasculopathy, CRV; or hereditary vascular retinopathy...
    17 KB (1,801 words) - 21:49, 17 January 2025
  • various pathologies, including neuropathologies, such as metachromatic leukodystrophy, Alzheimer's disease, and Parkinson's disease. Sulfatide is also associated...
    45 KB (5,620 words) - 11:53, 17 November 2024
  • syndrome Giant cell arteritis Giant cell inclusion disease Globoid cell leukodystrophy Gray matter heterotopia Guillain–Barré syndrome Head injury Headache...
    13 KB (1,143 words) - 17:54, 21 January 2025
  • enzyme that was studied in patients with late infantile metachromatic leukodystrophy, but found to be ineffective under the conditions of that trial. A subsequent...
    2 KB (199 words) - 07:39, 28 June 2024
  • galactocerebrosidase improves survival in a mouse model of globoid cell leukodystrophy". FASEB J. 21 (10): 2520–2527. doi:10.1096/fj.06-6169com. PMID 17403939...
    8 KB (989 words) - 19:48, 3 November 2024
  • Thumbnail for Leonor Varela
    Luna Mae, was born on 25 February 2015. Matteo was diagnosed with leukodystrophy (specifically an AGS) shortly after his birth. He died at the age of...
    11 KB (523 words) - 19:40, 6 March 2025
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