carnitine 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)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Miller, JL | 1 |
| Lynn, CH | 1 |
| Shuster, J | 1 |
| Driscoll, DJ | 1 |
| Ma, Y | 1 |
| Wu, T | 1 |
| Liu, Y | 1 |
| Wang, Q | 1 |
| Song, J | 1 |
| Song, F | 1 |
| Yang, Y | 1 |
2 other studies available for carnitine and Prader-Willi Syndrome
| Article | Year |
|---|---|
Carnitine and coenzyme Q10 levels in individuals with Prader-Willi syndrome.
Topics: Carnitine; Case-Control Studies; Child; Female; Humans; Male; Prader-Willi Syndrome; Siblings; Ubiqu | 2011 |
Nutritional and metabolic findings in patients with Prader-Willi syndrome diagnosed in early infancy.
Topics: Arginine; Carboxylic Acids; Carnitine; Chromosomes, Human, Pair 15; Diet Therapy; Early Diagnosis; F | 2012 |