Epidermolysis Bullosa, Junctional
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.
Year introduced: 1991
PubMed search builder options
Subheadings:
Tree Number(s): C16.131.831.493.170, C16.320.850.275.170, C17.800.804.493.170, C17.800.827.275.170, C17.800.865.410.170
MeSH Unique ID: D016109
Entry Terms:
- Junctional Epidermolysis Bullosa
- Epidermolysis Bullosa Junctionalis, Disentis Type
- Epidermolysis Bullosa Junctionalis, Severe Nonlethal
- Epidermolysis Bullosa, Generalized Atrophic Benign
- Epidermolysis Bullosa Progressiva
- Epidermolysis Bullosa Junctionalis, Progressive
- Epidermolysis Bullosa Letalis
- Bullosa Letali, Epidermolysis
- Bullosa Letalis, Epidermolysis
- Epidermolysis Bullosa Letali
- Letali, Epidermolysis Bullosa
- Letalis, Epidermolysis Bullosa
- Herlitz's Disease
- Disease, Herlitz's
- Herlitzs Disease
- Herlitz Disease
- Disease, Herlitz
- Lethal Junctional Epidermolysis Bullosa
- Epidermolysis Bullosa, Junctional, Herlitz-Pearson Type
- Epidermolysis Bullosa, Junctional, Herlitz Type
- Herlitz-Pearson Type Epidermolysis Bullosa
- Herlitz Pearson Type Epidermolysis Bullosa
- Epidermolysis Bullosa Junctionalis, Herlitz Type
- Herlitz-Pearson-Type Epidermolysis Bullosa
- Bullosa, Herlitz-Pearson-Type Epidermolysis
- Epidermolysis Bullosa, Herlitz-Pearson-Type
Previous Indexing: