Epidermolysis bullosa (EB) is a clinically and genetically heterogeneous group of inherited
blistering diseases that affects~ 500,000 people worldwide. Clinically, individuals with EB …

Dystrophic epidermolysis bullosa (DEB) is one of the major types of EB, a rare hereditary
group of trauma-induced blistering skin disorders. DEB is caused by inherited pathogenic …

Background Recessive dystrophic epidermolysis bullosa (RDEB) is a rare, devastating
blistering genodermatosis caused by mutations in the COL7A1 gene, which encodes for …

The dystrophic forms of epidermolysis bullosa are a group of inherited blistering disorders
caused by mutations in the type VII collagen gene (COL7A1). 1 Recessive dystrophic …

Dystrophic epidermolysis bullosa (DEB) is an epidermolysis bullosa (EB) subtype with rather
well understood pathogenesis. Its molecular basis—abnormalities of collagen VII—has been …

Dystrophic epidermolysis bullosa (DEB) is a severe skin fragility disorder associated with
trauma-induced blistering, progressive soft tissue scarring, and increased risk of skin cancer …

Dystrophic epidermolysis bullosa is a rare inherited blistering disorder caused by mutations
in the COL7A1 gene encoding type VII collagen. The deficiency and/or dysfunction of type …

Background/objective Recessive dystrophic epidermolysis bullosa (RDEB) is a genetic
collagen disorder characterized by skin fragility leading to blistering, wounds, and scarring …

Patients with recessive dystrophic epidermolysis bullosa (RDEB) have incurable skin
fragility, blistering, and scarring due to mutations in the gene that encodes for type VII …

Epidermolysis bullosa, a group of heritable blistering disorders, shows extensive phenotypic
variability due to mutations in as many as 20 distinct genes. There is no cure for this …