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Epidermolysis Bullosa, Junctional

More information in Books or onNLM PubMed
Definition: 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.      Other names Lethal Junctional Epidermolysis Bullosa; Junctional Epidermolysis Bullosa; Herlitz Disease; Epidermolysis Bullosa Letalis; Letalis, Epidermolysis Bullosa; Letali, Epidermolysis Bullosa; Herlitzs Disease; Herlitz Pearson Type Epidermolysis Bullosa; Epidermolysis Bullosa Letali; Disease, Herlitz's; Disease, Herlitz; Bullosa Letalis, Epidermolysis; Bullosa Letali, Epidermolysis; Herlitz-Pearson Type Epidermolysis Bullosa; Epidermolysis Bullosa, Junctional, Herlitz-Pearson; Epidermolysis Bullosa, Junctional, Herlitz Type; Epidermolysis Bullosa, Generalized Atrophic Benign; Herlitz's Disease; Epidermolysis Bullosa Progressiva; Epidermolysis Bullosa Junctionalis, Severe Nonleth
 
SubstanceCAS Registry & nameCategoriesSource
Epidermolysis bullosa inversa dystrophica  0   *Epidermolysis Bullosa, Junctional.
19-DEJ-1 antigen  0   *Antigens Epidermolysis Bullosa, Junctional. J Am Acad Dermatol 1994 Sep;31(3 Pt 1):429-33

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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