Übersetzung für 'erythroderma' von Englisch nach Deutsch

erythroderma

Erythroderm {n}med.

Erythrodermie {f}med.

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bullous congenital ichthyosiform erythroderma <BCIE>

Erythrodermia congenitalis ichthyosiformis bullosa {n}med.

• Deletions of "Alox12b" or "AloxE2" genes in mice cause a congenital scaly skin disease which is characterized by a greatly reduced skin water barrier function and is similar in other ways to the autosomal recessive nonbullous Congenital ichthyosiform erythroderma (ARCI) disease of humans.
• The incidence of erythroderma is estimated to be 1–2 in 100,000. While erythroderma can occur at any age, it is most common in older, male adults.
• The advanced stage of mycosis fungoides is characterized by generalized erythroderma (red rash covering most of the body) with severe pruritus (itching) and scaling.
• "Epitoxis erythroderma" is a moth of the subfamily Arctiinae. It was described by Per Olof Christopher Aurivillius in 1925 and is found in the Democratic Republic of the Congo.
• Less severe mutations result in a collodion membrane and congenital ichthyosiform erythroderma-like presentation.

• Leiner's disease is a systemic disease, a skin disorder and extends to erythroderma, typically diagnosed in early infancy.
• Increased transepidermal water loss resulting from the disturbance of corneocyte barrier function in erythroderma may cause profound metabolic abnormalities and hypernatremia, particularly in neonates.
• The first case of Neutral Lipid Storage Disease was reported by Maurice Dorfman when he treated two sisters with non bullous ichthyosiform erythroderma in 1974.
• Some of the most severe and life-threatening examples of drug eruptions are erythema multiforme, Stevens–Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), hypersensitivity vasculitis, drug induced hypersensitivity syndrome (DIHS), erythroderma and acute generalized exanthematous pustulosis (AGEP).