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.
推出的年份: 1991
树号: 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 单一 ID: D016109
进入的组:
Epidermolysis Bullosa, Generalized Atrophic Benign
Epidermolysis Bullosa Junctionalis, Severe Nonlethal
Junctional Epidermolysis Bullosa
Epidermolysis Bullosa Junctionalis, Disentis Type
Epidermolysis Bullosa Letalis
Bullosa Letali, Epidermolysis
Bullosa Letalis, Epidermolysis
Epidermolysis Bullosa Letali
Letali, Epidermolysis Bullosa
Letalis, Epidermolysis Bullosa
Herlitz Disease
Disease, Herlitz
Lethal Junctional Epidermolysis Bullosa
Herlitz-Pearson-Type Epidermolysis Bullosa
Bullosa, Herlitz-Pearson-Type Epidermolysis
Epidermolysis Bullosa, Herlitz-Pearson-Type
Epidermolysis Bullosa, Junctional, Herlitz Type
Herlitz-Pearson Type Epidermolysis Bullosa
Herlitz Pearson Type Epidermolysis Bullosa
Epidermolysis Bullosa Junctionalis, Herlitz Type
Herlitz's Disease
Disease, Herlitz's
Herlitzs Disease
Epidermolysis Bullosa, Junctional, Herlitz-Pearson Type
Epidermolysis Bullosa Progressiva
Epidermolysis Bullosa Junctionalis, Progressive
早前的内容:
Epidermolysis Bullosa (1966-1990)
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