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©The Author(s) 2025.
World J Stem Cells. Oct 26, 2025; 17(10): 109942
Published online Oct 26, 2025. doi: 10.4252/wjsc.v17.i10.109942
Published online Oct 26, 2025. doi: 10.4252/wjsc.v17.i10.109942
Table 1 Baseline characteristics of study participants, n (%)
| Characteristic | Value |
| Total patients, n | 50 |
| Age, mean ± SD (range), years | 8.7 ± 3.2 (3-15) |
| Sex | |
| Male | 28 (56) |
| Female | 22 (44) |
| Diagnosis | |
| Congenital anosmia | 32 (64) |
| Severe congenital hyposmia | 15 (30) |
| Kallmann syndrome | 3 (6) |
| Genetic mutations identified | 18 (36) |
| Baseline composite olfactory score, mean ± SD | 8.3 ± 4.7 |
Table 2 Changes in olfactory function components over 3-year follow-up, mean ± SD
| Component | Baseline | 3-year follow-up | P value |
| Odor threshold | 1.2 ± 0.8 | 6.8 ± 2.3 | < 0.001 |
| Odor discrimination | 3.1 ± 1.5 | 10.4 ± 3.1 | < 0.001 |
| Odor identification | 4.0 ± 2.4 | 35.4 ± 13.5 | < 0.001 |
- Citation: Ni X, Shi J, Ning J, Tian XL. Long-term follow-up of autologous nasal epithelial stem cell transplantation for congenital olfactory disorders in children. World J Stem Cells 2025; 17(10): 109942
- URL: https://www.wjgnet.com/1948-0210/full/v17/i10/109942.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v17.i10.109942
