acitretin has been researched along with Deafness in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cheong, SL; Coelho, R; Silva, G; Yau, SL | 1 |
| Handa, S; Kaur, I; Kumar, B; Radotra, BD; Sahoo, B | 1 |
| Bondeson, ML; Gunnarsson, U; Nyström, AM; Vahlquist, A | 1 |
| He, Y; Li, C; Luo, Q; Zhang, X; Zhou, H | 1 |
4 other study(ies) available for acitretin and Deafness
| Article | Year |
|---|---|
Unusual cutaneous manifestations and congenital hearing loss in a patient with GJB2 (F142L) mutation.
Topics: Acitretin; Adalimumab; Combined Modality Therapy; Connexin 26; Deafness; Dermatologic Agents; Humans; Male; Mutation; Skin Diseases; Skin Transplantation; Young Adult | 2021 |
KID syndrome: response to acitretin.
Topics: Acitretin; Adolescent; Alopecia; Deafness; Female; Humans; Ichthyosis; Keratitis; Keratolytic Agents; Syndrome | 2002 |
Connexin 26 (GJB2) mutations in two Swedish patients with atypical Vohwinkel (mutilating keratoderma plus deafness) and KID syndrome both extensively treated with acitretin.
Topics: Acitretin; Administration, Oral; Adult; Aged; Connexin 26; Connexins; Deafness; Female; Humans; Ichthyosis; Keratitis; Keratoderma, Palmoplantar; Keratolytic Agents; Male; Mutation; Syndrome | 2006 |
Severe ichthyosis-related disorders in children: response to acitretin.
Topics: Acitretin; Administration, Oral; Adolescent; Child; Child, Preschool; Deafness; Diagnosis, Differential; Female; Humans; Ichthyosiform Erythroderma, Congenital; Keratolytic Agents; Male; Severity of Illness Index; Syndrome | 2007 |