melatonin has been researched along with Acrocallosal Syndrome in 1 studies
Acrocallosal Syndrome: Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL ABNORMALITIES; digital malformations, and growth retardation.
| 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Duman, O | 1 |
| Durmaz, E | 1 |
| Akcurin, S | 1 |
| Serteser, M | 1 |
| Haspolat, S | 1 |
1 other study available for melatonin and Acrocallosal Syndrome
| Article | Year |
|---|---|
Spontaneous endogenous hypermelatoninemia: a new disease?
Topics: Acrocallosal Syndrome; Adrenergic beta-Antagonists; Agenesis of Corpus Callosum; Child; Female; Huma | 2010 |