pyridoxine has been researched along with Monosomy in 1 studies
4,5-bis(hydroxymethyl)-2-methylpyridin-3-ol: structure in first source
vitamin B6 : Any member of the group of pyridines that exhibit biological activity against vitamin B6 deficiency. Vitamin B6 deficiency is associated with microcytic anemia, electroencephalographic abnormalities, dermatitis with cheilosis (scaling on the lips and cracks at the corners of the mouth) and glossitis (swollen tongue), depression and confusion, and weakened immune function. Vitamin B6 consists of the vitamers pyridoxine, pyridoxal, and pyridoxamine and their respective 5'-phosphate esters (and includes their corresponding ionized and salt forms).
Monosomy: The condition in which one chromosome of a pair is missing. In a normally diploid cell it is represented symbolically as 2N-1.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The case history of two sisters with pyridoxine-refractory familial sideroblastic anemia (FSA) is presented in which one developed a myelodysplastic syndrome (MDS) with monosomy for chromosome 5." | 3.69 | Familial sideroblastic anemia with emergence of monosomy 5 and myelodysplastic syndrome. ( de Waal, FC; Kardos, G; Slater, R; van Oudheusden, LJ; Veerman, AJ, 1996) |
| 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 |
|---|---|
| Kardos, G | 1 |
| Veerman, AJ | 1 |
| de Waal, FC | 1 |
| van Oudheusden, LJ | 1 |
| Slater, R | 1 |
1 other study available for pyridoxine and Monosomy
| Article | Year |
|---|---|
Familial sideroblastic anemia with emergence of monosomy 5 and myelodysplastic syndrome.
Topics: Anemia, Refractory, with Excess of Blasts; Anemia, Sideroblastic; Child; Chromosomes, Human, Pair 5; | 1996 |