bullous erythroderma - definitie. Wat is bullous erythroderma
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Wat (wie) is bullous erythroderma - definitie

RARE AND SEVERE FORM OF ICHTHYOSIS
Bullous congenital ichthyosiform erythroderma; Hyperkeratosis, epidermolytic; Congenital bullous ichthyosiform erythroderma; Bullous Ichthyosis; Epidermolytic hyperkeratosis (Bullous ichthyosiform erythroderma); Bullous ichthyosiform erythroderma; Epidermolytic palmoplantar keratoderma; EHK; Mosaic bullous congenital ichthyosiform erythroderma; Linear bullous ichthyosiform erythroderma; Epidermolytic ichthyosis

Epidermolytic hyperkeratosis         
Epidermolytic ichthyosis (EI), also known as bullous epidermis ichthyosis (BEI), epidermolytic hyperkeratosis (EHK), bullous congenital ichthyosiform erythroderma (BCIE), bullous ichthyosiform erythrodermaFreedberg, et al. (2003).
Bullous pemphigoid         
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AUTOIMMUNE DISEASE OF SKIN AND CONNECTIVE TISSUE CHARACTERIZED BY LARGE BLISTERS
Pemphigoid, bullous; Bullous Pemphigoid; Bullous pemphigoid versus
Bullous pemphigoid (type of pemphigoid) is an autoimmune pruritic skin disease which typically occurs in people aged over 60, that may involve the formation of blisters (bullae) in the space between the epidermal and dermal skin layers. It is classified as a type II hypersensitivity reaction, which involves formation of anti-hemidesmosome antibodies, causing a loss of keratinocytes to basement membrane adhesion.
Bullous keratopathy         
HUMAN DISEASE
Bullour keratopathy; Pseudophakic bullous keratopathy
Bullous keratopathy, also known as pseudophakic bullous keratopathy (PBK), is a pathological condition in which small vesicles, or bullae, are formed in the cornea due to endothelial dysfunction.

Wikipedia

Epidermolytic hyperkeratosis

Epidermolytic ichthyosis (EI), also known as bullous epidermis ichthyosis (BEI), epidermolytic hyperkeratosis (EHK), bullous congenital ichthyosiform erythroderma (BCIE), bullous ichthyosiform erythroderma: 482  or bullous congenital ichthyosiform erythroderma Brocq, is a rare and severe form of ichthyosis that affects around 1 in 300,000 people. It is caused by a genetic mutation, and thus cannot be completely cured without some form of gene therapy.

While some research has been done into possible gene therapy treatments, the work hasn't yet been successfully developed to the stage where it can be routinely given to patients.

The condition involves the clumping of keratin filaments.: 562