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Junctional epidermolysis bullosa

Introduction: Junctional epidermolysis bullosa

Description of Junctional epidermolysis bullosa

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.
Source: Diseases Database

Junctional epidermolysis bullosa: Related Topics

These medical condition or symptom topics may be relevant to medical information for Junctional epidermolysis bullosa:

Junctional epidermolysis bullosa: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Junctional epidermolysis bullosa is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Junctional epidermolysis bullosa, or a subtype of Junctional epidermolysis bullosa, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Terms associated with Junctional epidermolysis bullosa:

Terms Similar to Junctional epidermolysis bullosa:

Source: Diseases Database

Source - NIH

External links related to: Junctional epidermolysis bullosa

Source: Diseases Database

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