Page last updated: 2024-10-24

caffeine and Leigh Disease

caffeine has been researched along with Leigh Disease in 1 studies

Leigh Disease: A group of metabolic disorders primarily of infancy characterized by the subacute onset of psychomotor retardation, hypotonia, ataxia, weakness, vision loss, eye movement abnormalities, seizures, dysphagia, and lactic acidosis. Pathological features include spongy degeneration of the neuropile of the basal ganglia, thalamus, brain stem, and spinal cord. Patterns of inheritance include X-linked recessive, autosomal recessive, and mitochondrial. Leigh disease has been associated with mutations in genes for the PYRUVATE DEHYDROGENASE COMPLEX; CYTOCHROME-C OXIDASE; ATP synthase subunit 6; and subunits of mitochondrial complex I. (From Menkes, Textbook of Child Neurology, 5th ed, p850).

Research

Studies (1)

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

Authors

AuthorsStudies
Mauron, A1

Other Studies

1 other study available for caffeine and Leigh Disease

ArticleYear
[Caffe lungo].
    Revue medicale suisse, 2013, Jun-05, Volume: 9, Issue:389

    Topics: Animals; Caffeine; Cattle; Cell Culture Techniques; Cell Transplantation; Cloning, Organism; Fibrobl

2013