halothane has been researched along with Prader-Willi Syndrome in 2 studies
Prader-Willi Syndrome: An autosomal dominant disorder caused by deletion of the proximal long arm of the paternal chromosome 15 (15q11-q13) or by inheritance of both of the pair of chromosomes 15 from the mother (UNIPARENTAL DISOMY) which are imprinted (GENETIC IMPRINTING) and hence silenced. Clinical manifestations include MENTAL RETARDATION; MUSCULAR HYPOTONIA; HYPERPHAGIA; OBESITY; short stature; HYPOGONADISM; STRABISMUS; and HYPERSOMNOLENCE. (Menkes, Textbook of Child Neurology, 5th ed, p229)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Aminophylline and steroid were administered intravenously and halothane was inhaled instead of sevoflurane." | 2.39 | [Bronchospasm during anesthesia in a patient with Prader-Willi syndrome]. ( Kawahito, S; Kimura, H; Kitahata, H; Kohyama, A, 1995) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 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 |
|---|---|
| Yamashita, M | 1 |
| Koishi, K | 1 |
| Yamaya, R | 1 |
| Tsubo, T | 1 |
| Matsuki, A | 1 |
| Oyama, T | 1 |
| Kawahito, S | 1 |
| Kitahata, H | 1 |
| Kimura, H | 1 |
| Kohyama, A | 1 |
1 review available for halothane and Prader-Willi Syndrome
| Article | Year |
|---|---|
[Bronchospasm during anesthesia in a patient with Prader-Willi syndrome].
Topics: Adrenergic beta-Agonists; Aminophylline; Anesthesia, General; Bronchial Spasm; Bronchodilator Agents | 1995 |
1 other study available for halothane and Prader-Willi Syndrome
| Article | Year |
|---|---|
Anaesthetic considerations in the Prader-Willi syndrome: report of four cases.
Topics: Anesthesia, Inhalation; Child; Cholelithiasis; Cryptorchidism; Female; Halothane; Humans; Infant; Ma | 1983 |