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Genotype-phenotype correlations on epidermolysis bullosa with congenital absence of skin: A comprehensive review.
Mariath LM, Santin JT, Frantz JA, Doriqui MJR, Schuler-Faccini L, Kiszewski AE. Mariath LM, et al. Clin Genet. 2021 Jan;99(1):29-41. doi: 10.1111/cge.13792. Epub 2020 Jun 29. Clin Genet. 2021. PMID: 32506467 Review.
Congenital absence of skin (CAS) is a clinical sign associated with the main types of epidermolysis bullosa (EB). Very few studies have investigated the genetic background that may influence the occurrence of this condition. ...A total of 171 cases (49 EB simplex, E …
Congenital absence of skin (CAS) is a clinical sign associated with the main types of epidermolysis bullosa (EB). Very few stu …
Epidermolysis bullosa dystrophica pretibialis - Clinical snapshot and management of a rare orphan disease.
Will LM, Reichrath J, Vogt T. Will LM, et al. J Dtsch Dermatol Ges. 2021 Jul;19(7):983-986. doi: 10.1111/ddg.14446. Epub 2021 May 5. J Dtsch Dermatol Ges. 2021. PMID: 33951274 Review.
If blistering occurs in childhood, the possibility of hereditary epidermolysis bullosa should be considered even if the symptoms are mild. Besides clinical and histological examination, molecular genetic screening is diagnostically relevant. For localized for …
If blistering occurs in childhood, the possibility of hereditary epidermolysis bullosa should be considered even if the sympto …
Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa.
Krämer S, Lucas J, Gamboa F, Peñarrocha Diago M, Peñarrocha Oltra D, Guzmán-Letelier M, Paul S, Molina G, Sepúlveda L, Araya I, Soto R, Arriagada C, Lucky AW, Mellerio JE, Cornwall R, Alsayer F, Schilke R, Antal MA, Castrillón F, Paredes C, Serrano MC, Clark V. Krämer S, et al. Spec Care Dentist. 2020 Nov;40 Suppl 1(Suppl 1):3-81. doi: 10.1111/scd.12511. Spec Care Dentist. 2020. PMID: 33202040 Free PMC article.
BACKGROUND: Inherited epidermolysis bullosa (EB) is a genetic disorder characterized by skin fragility and unique oral features. AIMS: To provide (a) a complete review of the oral manifestations in those living with each type of inherited EB, (b) the current best pr …
BACKGROUND: Inherited epidermolysis bullosa (EB) is a genetic disorder characterized by skin fragility and unique oral feature …
Autoimmune Subepidermal Bullous Diseases of the Skin and Mucosae: Clinical Features, Diagnosis, and Management.
Amber KT, Murrell DF, Schmidt E, Joly P, Borradori L. Amber KT, et al. Clin Rev Allergy Immunol. 2018 Feb;54(1):26-51. doi: 10.1007/s12016-017-8633-4. Clin Rev Allergy Immunol. 2018. PMID: 28779299 Review.
Autoimmune subepidermal blistering diseases of the skin and mucosae constitute a large group of sometimes devastating diseases, encompassing bullous pemphigoid, gestational pemphigoid, mucous membrane pemphigoid, epidermolysis bullosa acquisita, and anti-p200 pemphi …
Autoimmune subepidermal blistering diseases of the skin and mucosae constitute a large group of sometimes devastating diseases, encompassing …
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. The development of cutaneous squamous cell carcinomas (cSCCs) is one of the mos …
BACKGROUND: Hereditary epidermolysis bullosa (EB) is a rare genodermatosis characterized by skin fragility and blistering of t …
Mesenchymal stromal cells in wound healing applications: role of the secretome, targeted delivery and impact on recessive dystrophic epidermolysis bullosa treatment.
Riedl J, Popp C, Eide C, Ebens C, Tolar J. Riedl J, et al. Cytotherapy. 2021 Nov;23(11):961-973. doi: 10.1016/j.jcyt.2021.06.004. Epub 2021 Aug 8. Cytotherapy. 2021. PMID: 34376336 Free PMC article. Review.
Therefore, the specific mechanisms of how MSCs influence the local microenvironment in distinct wound etiologies warrant further research. ...Molecules released by the MSC secretome can promote re-epithelialization and angiogenesis while inhibiting fibrosis and microbial i …
Therefore, the specific mechanisms of how MSCs influence the local microenvironment in distinct wound etiologies warrant further rese …
Electrochemotherapy, a local treatment for squamous cell carcinoma in patients with recessive dystrophic epidermolysis bullosa.
Bartolo J, Farricha V, Carvalhal S, Moura C, Abecasis N. Bartolo J, et al. Dermatol Ther. 2020 Nov;33(6):e14093. doi: 10.1111/dth.14093. Epub 2020 Sep 7. Dermatol Ther. 2020. PMID: 32720460
Epidermolysis Bullosa (EB) is a rare group of diseases caused by genetic variants in skin structural proteins. EB is characterized by varying degrees of skin fragility, blisters and impaired wound healing, and is classified based on the ultrastructural levels of ski …
Epidermolysis Bullosa (EB) is a rare group of diseases caused by genetic variants in skin structural proteins. EB is character …