Epidermolysis bullosa, junctional, Herlitz-Pearson: A rare blistering skin disease which can often result in infant death. More detailed information about the symptoms, causes, and treatments of Epidermolysis bullosa, junctional, Herlitz-Pearson is available below.
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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)
Epidermolysis bullosa, junctional, Herlitz-Pearson is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Epidermolysis bullosa, junctional, Herlitz-Pearson, or a subtype of Epidermolysis bullosa, junctional, Herlitz-Pearson,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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