Clinicopathologic Types of Epidermolysis Bullosa and Their Nondermatological Complications
- 1 May 1988
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Dermatology
- Vol. 124 (5) , 718-725
- https://doi.org/10.1001/archderm.1988.01670050062023
Abstract
• 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)This publication has 5 references indexed in Scilit:
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- Dystrophic epidermolysis bullosa. A new variant characterized by progressive symmetrical centripetal involvement with scarringArchives of Dermatology, 1985
- Histopathologic and ultrastructural findings in certain genodermatosesClinics in Dermatology, 1985
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- Hereditary Epidermolysis Bullosa with Special Emphasis on Newly Recognized Syndromes and ComplicationsDermatologic Clinics, 1983