keratitis bullosa - significado y definición. Qué es keratitis bullosa
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Qué (quién) es keratitis bullosa - definición

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.
Exposure keratopathy         
HUMAN DISEASE
Exposure keratitis; Keratisis lagophthalmos
Exposure keratopathy (also known as exposure keratitis) is medical condition affecting the cornea of eyes. It can lead to corneal ulceration and permanent loss of vision due to corneal opacity.
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.

Wikipedia

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.