Page last updated: 2024-10-20

urea and Fragile X Syndrome

urea has been researched along with Fragile X Syndrome in 1 studies

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

Fragile X Syndrome: A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairment, hyperactivity, SEIZURES, language delay, and enlargement of the ears, head, and testes. INTELLECTUAL DISABILITY occurs in nearly all males and roughly 50% of females with the full mutation of FRAXA. (From Menkes, Textbook of Child Neurology, 5th ed, p226)

Research

Studies (1)

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

Authors

AuthorsStudies
Greicius, MD1
Boyett-Anderson, JM1
Menon, V1
Reiss, AL1

Other Studies

1 other study available for urea and Fragile X Syndrome

ArticleYear
Reduced basal forebrain and hippocampal activation during memory encoding in girls with fragile X syndrome.
    Neuroreport, 2004, Jul-19, Volume: 15, Issue:10

    Topics: Adolescent; Adult; Aged; Brain Mapping; Carbamide Peroxide; Case-Control Studies; Child; Cognition;

2004