Page last updated: 2024-10-17

creatine and Fragile X Syndrome

creatine has been researched along with Fragile X Syndrome in 2 studies

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 (2)

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

Authors

AuthorsStudies
Utine, GE1
Akpınar, B1
Arslan, U1
Kiper, PÖ1
Volkan-Salancı, B1
Alanay, Y1
Aktaş, D1
Haliloğlu, G1
Oğuz, KK1
Boduroğlu, K1
Alikaşifoğlu, M1
Kesler, SR1
Lightbody, AA1
Reiss, AL1

Trials

1 trial available for creatine and Fragile X Syndrome

ArticleYear
Cholinergic dysfunction in fragile X syndrome and potential intervention: a preliminary 1H MRS study.
    American journal of medical genetics. Part A, 2009, Volume: 149A, Issue:3

    Topics: Adolescent; Adult; Case-Control Studies; Choline; Cholinesterase Inhibitors; Cognition; Creatine; Do

2009

Other Studies

1 other study available for creatine and Fragile X Syndrome

ArticleYear
Neurochemical evaluation of brain function with 1H magnetic resonance spectroscopy in patients with fragile X syndrome.
    American journal of medical genetics. Part A, 2014, Volume: 164A, Issue:1

    Topics: Aspartic Acid; Brain; Case-Control Studies; Child; Child, Preschool; Choline; Creatine; Fragile X Sy

2014
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