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Epidermodysplasia verruciformis (EV) is a skin condition characterised by warty skin lesions. [1] It results from an abnormal susceptibility to HPV infection (HPV). It is associated with a high lifetime risk of squamous cell carcinomas in skin . [ 1 ]
Epidermodysplasia verruciformis is different in that it leaves victims unable to fight off certain types of HPV. "Tree man" syndrome is so rare that only 200 cases have been reported globally.
Epidermodysplasia verruciformis + Recessive dystrophic epidermolysis bullosa + Ferguson–Smith syndrome + Muir–Torre syndrome + + Nevoid basal cell carcinoma syndrome + Bazex syndrome + Rombo syndrome + Discoid lupus erythematosus + Erosive lichen planus + Lichen sclerosus + Porokeratosis + Nevus sebaceous [note 1] + Chronic non-healing ...
Epidermolysis bullosa intraepidermic; Epidermolysis bullosa inversa dystrophica; Epidermolysis bullosa simplex with anodontia, hair; Epidermolysis bullosa simplex, Cockayne–Touraine type; Epidermolysis bullosa simplex, Koebner type; Epidermolysis bullosa simplex, Ogna type; Epidermolysis bullosa, dermolytic; Epidermolysis bullosa, generalized ...
Acrokeratosis verruciformis ... disease, Herlitz epidermolysis bullosa, ... eruptions are skin conditions of the palms and soles which are resistant to treatment. [34]
Epidermolysis bullosa dystrophica or dystrophic EB (DEB) is an inherited disease affecting the skin and other organs. [ 1 ] [ 2 ] "Butterfly child" is the colloquial name for children born with the disease, as their skin is seen to be as delicate and fragile as the wings of a butterfly.
Formic acid, topical, is a common treatment for plantar warts, which works by being applied over a period of time, causing the body to reject the wart. [ 17 ] Fluorouracil cream, a chemotherapy agent sometimes used to treat skin cancer , can be used on particularly resistant warts, by blocking viral DNA and RNA production and repair.
Mitis junctional epidermolysis bullosa (also known as "Nonlethal junctional epidermolysis bullosa") is a skin condition characterized by scalp and nail lesions, also associated with periorificial nonhealing erosions. [1]: 599 Mitis junctional epidermolysis bullosa is most commonly seen in children between the ages of 4 and 10 years old.