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caffeine and Rett Syndrome

caffeine has been researched along with Rett Syndrome in 1 studies

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
"Chromosome analyses of lymphocytes cultured in a medium supplemented with caffeine showed a significantly higher frequency of fragile X(p22) in 13 girls with the Rett syndrome (RS) than in 9 healthy controls (p less than 0."7.68The Rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte culture. ( Anvret, M; Mellquist, L; Oden, A; Wahlström, J; Witt-Engerström, I, 1990)
"Chromosome analyses of lymphocytes cultured in a medium supplemented with caffeine showed a significantly higher frequency of fragile X(p22) in 13 girls with the Rett syndrome (RS) than in 9 healthy controls (p less than 0."3.68The Rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte culture. ( Anvret, M; Mellquist, L; Oden, A; Wahlström, J; Witt-Engerström, I, 1990)

Research

Studies (1)

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

Authors

AuthorsStudies
Wahlström, J1
Witt-Engerström, I1
Mellquist, L1
Anvret, M1
Oden, A1

Other Studies

1 other study available for caffeine and Rett Syndrome

ArticleYear
The Rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte culture.
    Brain & development, 1990, Volume: 12, Issue:1

    Topics: Adolescent; Adult; Caffeine; Cell Division; Cells, Cultured; Child; Child, Preschool; Female; Fragil

1990