Epidermolysis Bullosa

Epidermolysis bullosa is actually a group of disorders where there is blistering of the skin in response to minor trauma. These are inherited either as an autosomal dominant disease - only one damaged gene is necessary for you to develop the condition - or in a recessive manner, where both genes must be abnormal (one from each parent). The autosomal dominant disease is the milder of the two; infants with autosomal recessive epidermolysis bullosa may be severely affected. There is no treatment currently available.
 
 

This information is licensed for use by Wellbeing Information Systems Ltd ("WIS"), and protected by international copyright law. All rights are reserved. (email info@wisinfo.co.uk).
The information provided by WIS is for guidance only. Whilst it is based upon the expert advice of leading professionals, and extensive research, it is not a substitute for diagnosis by a qualified professional. Always consult your doctor, pharmacist or qualified practitioner before making any changes or additions to prescribed medication.