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Τι (ποιος) είναι Herlitz-type epidermolysis bullosa - ορισμός
DISORDER RESULTING FROM MUTATIONS IN THE GENES ENCODING KERATIN 5 OR KERATIN 14
Weber-Cockayne syndrome; Epidermolysis Bullosa Simplex, Generalized; Epidermolysis Bullosa Simplex, Localized; Generalized epidermolysis bullosa simplex; Koebner variant of generalized epidermolysis bullosa simplex; Localized epidermolysis bullosa simplex; Weber-Cockayne variant of generalized epidermolysis bullosa simplex; Epidermolysis bullosa herpetiformis; Dowling–Meara epidermolysis bullosa simplex; Epidermolysis bullosa simplex of Ogna; Epidermolysis bullosa simplex with muscular dystrophy; Epidermolysis bullosa simplex with mottled pigmentation; Weber–Cockayne syndrome; Weber–Cockayne variant of generalized epidermolysis bullosa simplex; Dowling-Meara epidermolysis bullosa simplex; Epidermolysis bullosa simplex (Köbner); Epidermolysis bullosa simplex with mottled pigmentation (Gedde-Dahl); Epidermolysis bullosa simplex (Weber-Cockayne); Dowling-Meara disease; Epidermolysis bullosa simplex herpetiformis
Epidermolysis bullosa dystrophica
INHERITED DISEASE AFFECTING THE SKIN AND OTHER ORGANS
Dystrophic Epidermolysis Bullosa; Dystrophic epidermolysis bullosa; Dominant dystrophic epidermolysis bullosa; Cockayne-Touraine disease; Recessive dystrophic epidermolysis bullosa; Hallopeau-Siemens variant of epidermolysis bullosa; Hallopeau–Siemens disease; Hallopeau-Siemens disease; Hallopeau–Siemens variant of epidermolysis bullosa; Dystrophic - dominant (Pasini variant) epidermolysis bullosa; Dystrophic - inverse epidermolysis bullosa; Dystrophic - generalised recessive (Hallopeau-Siemens) epidermolysis bullosa
Epidermolysis bullosa dystrophica or dystrophic EB (DEB) is an inherited disease affecting the skin and other organs.
Epidermolysis bullosa acquisita
CHRONIC SUBEPIDERMAL BLISTERING DISEASE ASSOCIATED WITH AUTOIMMUNITY TO TYPE VII COLLAGEN
Epidermolysis acquisata; Acquired epidermolysis bullosa; Drug-induced epidermolysis bullosa acquisita; Epidermolysis acquisata due to drug
Epidermolysis bullosa acquisita, also known as acquired epidermolysis bullosa, is a longterm autoimmune blistering skin disease. It generally presents with fragile skin that blisters and becomes red with or without trauma.
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex (EBS) is a disorder resulting from mutations in the genes encoding keratin 5 or keratin 14.Freedberg, et al.
Βικιπαίδεια
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex (EBS) is a disorder resulting from mutations in the genes encoding keratin 5 or keratin 14.: 598
Epidermolysis bullosa simplex (EBS) is one of the major forms of epidermolysis bullosa, a group of genetic conditions that cause the skin to be very fragile and to blister easily. Blister formation of EBS occurs at the dermal-epidermal junction.
