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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 2
2003 1
2006 1
2010 3
2011 2
2013 3
2014 4
2015 4
2016 2
2019 4
2020 1
2021 3
2022 9
2023 4
2024 2

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37 results

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Page 1
Update in the Management of Basal Cell Carcinoma.
Basset-Seguin N, Herms F. Basset-Seguin N, et al. Acta Derm Venereol. 2020 Jun 3;100(11):adv00140. doi: 10.2340/00015555-3495. Acta Derm Venereol. 2020. PMID: 32346750 Free PMC article. Review.
Ultraviolet (UV) exposure is the major carcinogenic factor. Some genodermatosis can predispose to formation of basal cell carcinomas at an earlier age. ...
Ultraviolet (UV) exposure is the major carcinogenic factor. Some genodermatosis can predispose to formation of basal cell carcinomas …
Therapeutic Options for the Treatment of Darier's Disease: A Comprehensive Review of the Literature.
Hanna N, Lam M, Fleming P, Lynde CW. Hanna N, et al. J Cutan Med Surg. 2022 May-Jun;26(3):280-290. doi: 10.1177/12034754211058405. Epub 2021 Nov 28. J Cutan Med Surg. 2022. PMID: 34841914 Free PMC article. Review.
However, a variety of treatments have been proposed in the literature including retinoids, steroids, vitamin D analogs, photodynamic therapy, and surgical excision. The purpose of this review article is to identify therapeutic options for treating DD and to outline …
However, a variety of treatments have been proposed in the literature including retinoids, steroids, vitamin D analogs, photodynamic ther …
Dupilumab in the treatment of genodermatosis: A systematic review.
Wu PC, Dai YX, Li CL, Chen CC, Chang YT, Ma SH. Wu PC, et al. J Dtsch Dermatol Ges. 2023 Jan;21(1):7-17. doi: 10.1111/ddg.14924. Epub 2023 Jan 19. J Dtsch Dermatol Ges. 2023. PMID: 36657040 Review.
Specific genodermatoses, including Netherton syndrome, epidermolysis bullosa pruriginosa, and hyper-IgE syndrome, are Th2 skewed diseases with activation of type 2 inflammation. We performed this systematic review to investigate the therapeutic role of dupilumab in the tre …
Specific genodermatoses, including Netherton syndrome, epidermolysis bullosa pruriginosa, and hyper-IgE syndrome, are Th2 skewed diseases wi …
Ichthyosis with confetti: clinics, molecular genetics and management.
Guerra L, Diociaiuti A, El Hachem M, Castiglia D, Zambruno G. Guerra L, et al. Orphanet J Rare Dis. 2015 Sep 17;10:115. doi: 10.1186/s13023-015-0336-4. Orphanet J Rare Dis. 2015. PMID: 26381864 Free PMC article. Review.
However, the hallmark of the disease is the appearance, in childhood or later in life, of healthy skin confetti-like spots, which increase in number and size with time. IWC is a very rare genodermatosis, with a prevalence <1/1,000,000 and only 40 cases reported worldwid …
However, the hallmark of the disease is the appearance, in childhood or later in life, of healthy skin confetti-like spots, which increase i …
Hailey-Hailey disease and review of management.
Chiaravalloti A, Payette M. Chiaravalloti A, et al. J Drugs Dermatol. 2014 Oct;13(10):1254-7. J Drugs Dermatol. 2014. PMID: 25607561 Review.
IMPORTANCE: Hailey-Hailey disease, or familial benign chronic pemphigus, is a rare genodermatosis that can be challenging for both patients and dermatologists as the disease can significantly impact patients' quality of life and is often difficult to control. ...OBJECTIVE: …
IMPORTANCE: Hailey-Hailey disease, or familial benign chronic pemphigus, is a rare genodermatosis that can be challenging for both pa …
Genetic and developmental disorders of the oral mucosa: Epidemiology; molecular mechanisms; diagnostic criteria; management.
Pinna R, Cocco F, Campus G, Conti G, Milia E, Sardella A, Cagetti MG. Pinna R, et al. Periodontol 2000. 2019 Jun;80(1):12-27. doi: 10.1111/prd.12261. Periodontol 2000. 2019. PMID: 31090139 Review.
This review describes chondro-ectodermal dysplasia, dyskeratosis congenita, Ehlers-Danlos syndrome, hereditary benign intraepithelial dyskeratosis, keratosis follicularis, lipoid proteinosis, multiple hamartoma syndrome, pachyonychia congenita, Peutz-Jeghers syndrome, tuberous sc …
This review describes chondro-ectodermal dysplasia, dyskeratosis congenita, Ehlers-Danlos syndrome, hereditary benign intraepithelial dysker …
Surgical management and oncological follow-up of cutaneous squamous cell carcinomas arising in epidermolysis bullosa patients.
Paganelli A, Giordano E, Fiorentini C, Ferrari B, Reggiani C, Garbarino F, Magnoni C. Paganelli A, et al. Int J Dermatol. 2022 Oct;61(10):1171-1174. doi: 10.1111/ijd.16157. Epub 2022 Mar 22. Int J Dermatol. 2022. PMID: 35315931 Free PMC article.
BACKGROUND: Hereditary epidermolysis bullosa (EB) is a rare genodermatosis characterized by skin fragility and blistering of the skin and mucous membranes in reaction to minimal traumas. ...However, not only recognition of cSCCs can be challenging in the affected skin but …
BACKGROUND: Hereditary epidermolysis bullosa (EB) is a rare genodermatosis characterized by skin fragility and blistering of the skin …
Application of topical gentamicin-a new era in the treatment of genodermatosis.
Wang S, Yang Z, Liu Y, Zhao MT, Zhao J, Zhang H, Liu ZY, Wang XL, Ma L, Yang YH. Wang S, et al. World J Pediatr. 2021 Dec;17(6):568-575. doi: 10.1007/s12519-021-00469-2. Epub 2021 Nov 17. World J Pediatr. 2021. PMID: 34787828 Review.
However, in the past decade, there were considerable interests in therapeutic approaches in treating hereditary diseases. Some of the genodermatosis is caused by nonsense mutations that create premature termination codons and lead to the production of truncated or n …
However, in the past decade, there were considerable interests in therapeutic approaches in treating hereditary diseases. Some of the …
The NF1 microdeletion syndrome: early genetic diagnosis facilitates the management of a clinically defined disease.
Kehrer-Sawatzki H, Bäzner U, Krämer J, Lewerenz J, Pfeiffer C. Kehrer-Sawatzki H, et al. J Dtsch Dermatol Ges. 2022 Mar;20(3):273-277. doi: 10.1111/ddg.14707. Epub 2022 Mar 4. J Dtsch Dermatol Ges. 2022. PMID: 35246941 Review.
Neurofibromatosis type-1 (NF1) is a genodermatosis frequently encountered in general dermatology. In many patients, the diagnosis of NF1 is made clinically based on the presence of cafe-au-lait macules and skinfold freckling, as well as plexiform neurofibromas detectable d …
Neurofibromatosis type-1 (NF1) is a genodermatosis frequently encountered in general dermatology. In many patients, the diagnosis of …
37 results