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Concept information

Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Eczematous > Dermatitis, Atopic
Skin and Connective Tissue Diseases > Skin Diseases > Dermatitis > Dermatitis, Atopic
Immune System Diseases > Hypersensitivity > Hypersensitivity, Immediate > Dermatitis, Atopic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Dermatitis, Atopic
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Dermatitis, Atopic

Término preferido

Dermatitis, Atopic  

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Tipo

  • mesh:Descriptor

Definición

  • A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema.

Concepto genérico

Etiquetas alternativas

  • Eczema, Atopic
  • Neurodermatitis, Atopic
  • Neurodermatitis, Disseminated

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-VCLJ50XR-1

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