Epidermolysis bullosa hereditaria simplex. Case report

N. I. Kihiczak, A. J. Papadopoulos, R. A. Schwartz, C. K. Janniger

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3 Scopus citations


Blistering is a common childhood phenomenon. There is a group of heterogeneous, genetic mechanobullous diseases termed epidermolysis bullosa (EB) whose hallmark is blistering due to minor trauma or pressure. Some patients with EB may be limited in common extracurricular activities such as playing tennis or hiking, while others may be asymptomatic with occasional blistering. The level of vesiculation within the skin defines three major subtypes of EB: EB simplex, dystrophic EB and junctional EB. We describe a patient and review the simple type of epidermolysis bullosa (EBS), which has an incidence of approximately 10-30 cases per million. The incidence of EBS is most probably higher than the stated figure, due to underreporting of mild cases. The severity of EBS depends upon the type of underlying defect.

Original languageEnglish (US)
Pages (from-to)24-30
Number of pages7
JournalActa Dermatovenerologica Alpina, Panonica et Adriatica
Issue number1
StatePublished - 2001

All Science Journal Classification (ASJC) codes

  • Dermatology
  • Infectious Diseases


  • Blistering disorder
  • Child
  • Epidermolysis bullosa
  • Hereditary
  • Simplex


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