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glycerol and Adrenoleukodystrophy

glycerol has been researched along with Adrenoleukodystrophy in 1 studies

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Adrenoleukodystrophy: An X-linked recessive disorder characterized by the accumulation of saturated very long chain fatty acids in the LYSOSOMES of ADRENAL CORTEX and the white matter of CENTRAL NERVOUS SYSTEM. This disease occurs almost exclusively in the males. Clinical features include the childhood onset of ATAXIA; NEUROBEHAVIORAL MANIFESTATIONS; HYPERPIGMENTATION; ADRENAL INSUFFICIENCY; SEIZURES; MUSCLE SPASTICITY; and DEMENTIA. The slowly progressive adult form is called adrenomyeloneuropathy. The defective gene ABCD1 is located at Xq28, and encodes the adrenoleukodystrophy protein (ATP-BINDING CASSETTE TRANSPORTERS).

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hoefler, G1
Paschke, E1
Hoefler, S1
Moser, AB1
Moser, HW1

Other Studies

1 other study available for glycerol and Adrenoleukodystrophy

ArticleYear
Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damage.
    The Journal of clinical investigation, 1991, Volume: 88, Issue:6

    Topics: Adrenoleukodystrophy; Cell Survival; Cells, Cultured; Fatty Acids; Fibroblasts; Glycerol; Humans; Mi

1991