Antecedentes y objetivo: La epidermólisis bullosa (EB) es un grupo heterogéneo de
trastornos hereditarios caracterizado por un aumento de la fragilidad mucocutánea. El …

Résumé Les épidermolyses bulleuses héréditaires (EBH) sont un groupe hétérogène de
maladies génétiques rares caractérisées par une fragilité cutanée et/ou muqueuse …

Although rare genodermatoses such as Epidermolysis bullosa have received more attention
over the last years, no approved treatment options targeting causal mutations are currently …

Background The non-healing wound is a characteristic clinical sign in recessive dystrophic
epidermolysis bullosa (RDEB). Methods Six patients with recessive dystrophic …

Epidermolysis bullosa (EB) is a rare inherited group of mechanobullous genodermatoses. It
is known to be one of the most devastating chronic conditions due to its frequent and …

Врожденный буллезный эпидермолиз—группа наследственных заболеваний кожи,
обусловленных мутациями в генах структурных белков дермо-эпидермального …

Congenital epidermolysis bullosa is a group of hereditary skin diseases caused by
mutations in the genes of structural proteins of the dermoepidermal junction of the skin …

Cutaneous squamous cell carcinoma (cSCC) is one of the most prevalent neoplasms
worldwide. Important risk factors for cSCC include sun exposure, immunosuppression, pale …

The term “hereditary epidermolysis bullosa”(EB) covers clinically and genetically
heterogeneous diseases associated with blisters of the skin and mucous membranes after …

Resilient in health, the structural integrity of skin can become impaired or break down in a
collection of inherited skin diseases, referred to as the blistering genodermatoses. Most …