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The authors report a child who has a kindred affected with epidermolysis bullosa hereditaria
simplex over 5 generations.
Diagnosis was made on the. basis of family history, clinical maifestations, and histological findings
of the affected skin. The absence of dystrophic changes of the skin and mucous membrane is characteristic
of this tybe and gives a better prognosis than the dystrophis form. Trauma and... |