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propionic acid and Basal Ganglia Diseases

propionic acid has been researched along with Basal Ganglia Diseases in 2 studies

propionic acid : A short-chain saturated fatty acid comprising ethane attached to the carbon of a carboxy group.

Basal Ganglia Diseases: Diseases of the BASAL GANGLIA including the PUTAMEN; GLOBUS PALLIDUS; claustrum; AMYGDALA; and CAUDATE NUCLEUS. DYSKINESIAS (most notably involuntary movements and alterations of the rate of movement) represent the primary clinical manifestations of these disorders. Common etiologies include CEREBROVASCULAR DISORDERS; NEURODEGENERATIVE DISEASES; and CRANIOCEREBRAL TRAUMA.

Research Excerpts

ExcerptRelevanceReference
"We report a 5-year-old boy with propionic acidaemia who developed a rapidly fatal necrosis of the basal ganglia after an episode of clinical deterioration."3.70An unusual late-onset case of propionic acidaemia: biochemical investigations, neuroradiological findings and mutation analysis. ( Cabrera, JC; Gangoiti, J; García, MJ; Hoenicka, J; Martí, M; Merinero, B; Muro, S; Peña, L; Pérez-Cerdá, C; Richard, E; Rodríguez-Pombo, P; Sanz, P; Ugarte, M, 1998)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Pérez-Cerdá, C1
Merinero, B1
Martí, M1
Cabrera, JC1
Peña, L1
García, MJ1
Gangoiti, J1
Sanz, P1
Rodríguez-Pombo, P1
Hoenicka, J1
Richard, E1
Muro, S1
Ugarte, M1
Burlina, AP1
Baracchini, C1
Carollo, C1
Burlina, AB1

Other Studies

2 other studies available for propionic acid and Basal Ganglia Diseases

ArticleYear
An unusual late-onset case of propionic acidaemia: biochemical investigations, neuroradiological findings and mutation analysis.
    European journal of pediatrics, 1998, Volume: 157, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Basal Ganglia; Basal Ganglia Diseases; Carboxy-Lyases; Child,

1998
Propionic acidaemia with basal ganglia stroke: treatment of acute extrapyramidal symptoms with L-DOPA.
    Journal of inherited metabolic disease, 2001, Volume: 24, Issue:5

    Topics: Adolescent; Basal Ganglia Diseases; Humans; Levodopa; Magnetic Resonance Imaging; Male; Propionates;

2001