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)
Excerpt | Relevance | Reference |
---|---|---|
"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." | 7.68 | The 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." | 3.68 | The Rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte culture. ( Anvret, M; Mellquist, L; Oden, A; Wahlström, J; Witt-Engerström, I, 1990) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Wahlström, J | 1 |
Witt-Engerström, I | 1 |
Mellquist, L | 1 |
Anvret, M | 1 |
Oden, A | 1 |
1 other study available for caffeine and Rett Syndrome
Article | Year |
---|---|
The Rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte culture.
Topics: Adolescent; Adult; Caffeine; Cell Division; Cells, Cultured; Child; Child, Preschool; Female; Fragil | 1990 |