Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
2012 1
2013 1
2017 1
2021 2
2022 1
2023 3
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

9 results

Results by year

Filters applied: . Clear all
Page 1
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.
We performed this systematic review to investigate the therapeutic role of dupilumab in the treatment of genodermatosis. A systematic search was conducted of the PubMed, Embase, Web of Science, and Cochrane databases from inception to December 13, 2021. The review included …
We performed this systematic review to investigate the therapeutic role of dupilumab in the treatment of genodermatosis. A systematic …
Dental and oral anomalies in incontinentia pigmenti: a systematic review.
Minić S, Trpinac D, Gabriel H, Gencik M, Obradović M. Minić S, et al. Clin Oral Investig. 2013 Jan;17(1):1-8. doi: 10.1007/s00784-012-0721-5. Epub 2012 Mar 28. Clin Oral Investig. 2013. PMID: 22453515 Review.
OBJECTIVES: Incontinentia pigmenti (IP) is an X-linked genodermatosis caused by a mutation of the IKBKG gene. The objective of this study was to present a systematic review of the dental and oral types of anomalies, to determine the total number and sex distribution of the …
OBJECTIVES: Incontinentia pigmenti (IP) is an X-linked genodermatosis caused by a mutation of the IKBKG gene. The objective of this s …
Therapeutics of xeroderma pigmentosum: A PRISMA-compliant systematic review.
de Andrade FAG, Cavalcanti CEO, Isoldi FC, Ferreira LM. de Andrade FAG, et al. Indian J Dermatol Venereol Leprol. 2021 Mar-Apr;87(2):176-189. doi: 10.25259/IJDVL_431_19. Indian J Dermatol Venereol Leprol. 2021. PMID: 33769755 Free article.
Xeroderma pigmentosum is a rare hereditary autosomal recessive genodermatosis. At present, there are many treatment options for xeroderma pigmentosum, covering medical/procedural, surgical and combined modalities. ...
Xeroderma pigmentosum is a rare hereditary autosomal recessive genodermatosis. At present, there are many treatment options for xerod …
The impact of epidermolysis bullosa on the family and healthcare practitioners: a scoping review.
Chateau AV, Blackbeard D, Aldous C. Chateau AV, et al. Int J Dermatol. 2023 Apr;62(4):459-475. doi: 10.1111/ijd.16197. Epub 2022 May 7. Int J Dermatol. 2023. PMID: 35524482 Review.
BACKGROUND: Epidermolysis bullosa (EB) is an inherited genodermatosis that results in mucocutaneous fragility. There is a lack of data on the impact of this disease on parents. ...
BACKGROUND: Epidermolysis bullosa (EB) is an inherited genodermatosis that results in mucocutaneous fragility. There is a lack of dat …
Therapies for cutaneous squamous cell carcinoma in recessive dystrophic epidermolysis bullosa: a systematic review of 157 cases.
Hwang A, Kwon A, Miller CH, Reimer-Taschenbrecker A, Paller AS. Hwang A, et al. Orphanet J Rare Dis. 2024 May 21;19(1):206. doi: 10.1186/s13023-024-03190-1. Orphanet J Rare Dis. 2024. PMID: 38769503 Free PMC article. Review.
BACKGROUND: Invasive cutaneous squamous cell carcinomas (cSCC) are a leading cause of death in recessive dystrophic epidermolysis bullosa (RDEB), a rare blistering genodermatosis. Outcomes of RDEB-cSCC therapies have primarily been described in case reports. ...
BACKGROUND: Invasive cutaneous squamous cell carcinomas (cSCC) are a leading cause of death in recessive dystrophic epidermolysis bullosa (R …
(New) antenatal ultrasound signs of fetal junctional epidermolysis bullosa: A case report and systematic review of literature.
Tosto V, Herrero B, Illescas T, De la Calle Fernandez-Miranda M, Moreno-Sanz B, de Lucas R, Bartha JL, Antolin E. Tosto V, et al. Eur J Obstet Gynecol Reprod Biol. 2023 Nov;290:43-50. doi: 10.1016/j.ejogrb.2023.08.379. Epub 2023 Aug 24. Eur J Obstet Gynecol Reprod Biol. 2023. PMID: 37717401 Review.
Epidermolysis bullosa is a rare hereditary autosomal disease that is included in the heterogeneous group of genodermatosis. It is characterized by skin and mucous membranes fragility and denudation, and it can be associated with pyloric atresia. ...
Epidermolysis bullosa is a rare hereditary autosomal disease that is included in the heterogeneous group of genodermatosis. It is cha …
Novel TMC8 splice site mutation in epidermodysplasia verruciformis and review of HPV infections in patients with the disease.
Imahorn E, Yüksel Z, Spoerri I, Gürel G, Imhof C, Saraçoğlu ZN, Koku Aksu AE, Rady PL, Tyring SK, Kempf W, Itin PH, Burger B. Imahorn E, et al. J Eur Acad Dermatol Venereol. 2017 Oct;31(10):1722-1726. doi: 10.1111/jdv.14431. Epub 2017 Aug 4. J Eur Acad Dermatol Venereol. 2017. PMID: 28646613 Review.
BACKGROUND: Epidermodysplasia verruciformis (EV) is a genodermatosis leading to infections with cutaneous HPV, persistent plane warts and a high rate of non-melanoma skin cancer (NMSC). ...
BACKGROUND: Epidermodysplasia verruciformis (EV) is a genodermatosis leading to infections with cutaneous HPV, persistent plane warts …
Advances in treatment for lipoid proteinosis (Urbach-Wiethe disease): a case report and systematic review.
Bueno-Molina RC, Hernández-Rodríguez JC, Cabrera-Fuentes R, Cabrera-Pérez R, Conejo-Mir Sánchez J, Pereyra-Rodríguez JJ. Bueno-Molina RC, et al. Clin Exp Dermatol. 2024 May 21;49(6):547-555. doi: 10.1093/ced/llae039. Clin Exp Dermatol. 2024. PMID: 38308656
BACKGROUND: Lipoid proteinosis (LP), also known as Urbach-Wiethe disease, is a rare autosomal recessive genodermatosis, caused by mutations in the ECM1 gene. This results in the deposition of periodic acid-Schiff (PAS)-positive, hyaline-like material on the skin, mucosae a …
BACKGROUND: Lipoid proteinosis (LP), also known as Urbach-Wiethe disease, is a rare autosomal recessive genodermatosis, caused by mut …