• The various epidermolysis bullosa syndromes are classified into (1) epidermolytic, (2) lamina lucidolytic (junctional), and (3) dermolytic (dystrophic) subgroups. The mode of inheritance and the clinical manifestations, both cutaneous and noncutaneous, are systematically summarized. This report provides an overview of the diverse epidermolysis bullosa syndromes, particularly from the perspective of their nondermatological manifestations.
(Arch Dermatol 1988;124:718-725)
Pearson RW. Clinicopathologic Types of Epidermolysis Bullosa and Their Nondermatological Complications. Arch Dermatol. 1988;124(5):718–725. doi:10.1001/archderm.1988.01670050062023
Monkeypox Resource Center
Customize your JAMA Network experience by selecting one or more topics from the list below.