cytosine has been researched along with Hirschsprung Disease in 1 studies
Hirschsprung Disease: Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON.
| 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 |
|---|---|
| Müller, CM | 1 |
| Haase, MG | 1 |
| Kemnitz, I | 1 |
| Fitze, G | 1 |
1 other study available for cytosine and Hirschsprung Disease
| Article | Year |
|---|---|
Genetic mosaicism of a frameshift mutation in the RET gene in a family with Hirschsprung disease.
Topics: Adult; Aged; Alleles; Codon; Cytosine; DNA; DNA Mutational Analysis; Erythrocytes; Family Health; Fe | 2014 |