Junctional Epidermolysis Bullosa

Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is characterized by generalized blister formation, extensive denudation, and separation and cleavage of the basal cell plasma membranes from the basement membrane.

Also Known As:

Epidermolysis Bullosa Letalis; Epidermolysis Bullosa, Junctional; Epidermolysis Bullosa Progressiva; Herlitz's Disease; Herlitz Disease; Lethal Junctional Epidermolysis Bullosa

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Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 449

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Congenital Abnormalities: 10008

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Skin Abnormalities: 78

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Epidermolysis Bullosa: 383

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Junctional Epidermolysis Bullosa: 172

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Inborn Genetic Diseases: 578

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Genetic Skin Diseases: 11

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Epidermolysis Bullosa: 383

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Junctional Epidermolysis Bullosa: 172

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Skin and Connective Tissue Diseases

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Skin Diseases: 6187

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Vesiculobullous Skin Diseases: 223

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Epidermolysis Bullosa: 383

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Junctional Epidermolysis Bullosa: 172

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Skin Abnormalities: 78

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Epidermolysis Bullosa: 383

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Junctional Epidermolysis Bullosa: 172

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Genetic Skin Diseases: 11

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Epidermolysis Bullosa: 383

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Junctional Epidermolysis Bullosa: 172

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