Page last updated: 2024-10-21

urea and Rett Syndrome

urea has been researched along with Rett Syndrome in 3 studies

pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.

Rett Syndrome: An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The affected female is normal until the age of 6-25 months when progressive loss of voluntary control of hand movements and communication skills; ATAXIA; SEIZURES; autistic behavior; intermittent HYPERVENTILATION; and HYPERAMMONEMIA appear. (From Menkes, Textbook of Child Neurology, 5th ed, p199)

Research Excerpts

ExcerptRelevanceReference
"The in vivo functioning of the urea cycle in the Rett syndrome (RS) was investigated using alanine load test."7.68The urea cycle in the Rett syndrome. ( Hjelm, M; Oberholzer, V; Thomas, S; Wilson, J, 1990)
"The in vivo functioning of the urea cycle in the Rett syndrome (RS) was investigated using alanine load test."3.68The urea cycle in the Rett syndrome. ( Hjelm, M; Oberholzer, V; Thomas, S; Wilson, J, 1990)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Burd, L1
Kemp, R1
Knull, H1
Loveless, D1
Clarke, A1
Gardner-Medwin, D1
Richardson, J1
McGann, A1
Bonham, JR1
Carpenter, KH1
Bhattacharya, S1
Haggerty, D1
Fleetwood, JA1
Aynsley-Green, A1
Thomas, S1
Oberholzer, V1
Wilson, J1
Hjelm, M1

Reviews

1 review available for urea and Rett Syndrome

ArticleYear
A review of the biochemical pathways studied and abnormalities reported in the Rett syndrome.
    Brain & development, 1990, Volume: 12, Issue:4

    Topics: Biogenic Amines; Carnitine; Energy Metabolism; Glutarates; Goals; Humans; Neurotransmitter Agents; R

1990

Other Studies

2 other studies available for urea and Rett Syndrome

ArticleYear
Abnormalities of carbohydrate metabolism and of OCT gene function in the Rett syndrome.
    Brain & development, 1990, Volume: 12, Issue:1

    Topics: Adolescent; Carbohydrate Metabolism; Child; Child, Preschool; Female; Genetic Linkage; Humans; Metab

1990
The urea cycle in the Rett syndrome.
    Brain & development, 1990, Volume: 12, Issue:1

    Topics: Adult; Ammonia; Child; Child, Preschool; Female; Humans; Middle Aged; Orotic Acid; Rett Syndrome; Ur

1990