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About EB

What is EB

Inherited EB


Classification

What is Epidermolysis Bullosa?

Epidermolysis Bullosa, known as EB, is the name of a group of genetic disorders causing blistering and shearing of the skin from even the gentlest friction, often from everyday activities.  

Over twenty different sub types of EB have been identified, each with their own characteristic symptoms. EB can vary from a relatively mild condition to an incapacitating, and sometimes fatal, disorder.


What does the name mean?

The skin is made up of a number of different layers. The outer is called the epidermis; the inner layers are the dermis. "Bullosa" is simply the name for a blister and "lysis" means breakdown. Hence, Epidermolysis Bullosa means the breakdown and blistering of the epidermis.

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What causes the disease?


The understanding of the causes of EB has grown greatly over recent years. All forms of EB are genetic in origin and the genes responsible for several different sub types of the condition are now known. Others still await identification.
The genetic defects result in the skin layers not adhering properly to each other, causing areas of structural weakness. This fragile skin is
particularly vulnerable to damage from mild friction, causing the blisters which are the characteristic feature of the condition. Researchers are very optimistic about the possibility of developing treatments as knowledge about EB increases. DebRA is committed to ensuring that this optimism becomes a reality.

What are the symptoms of EB?

The various forms of EB can be grouped into three main types; EB Simplex, Dystrophic EB (dominant or recessive form) and Junctional EB. The severity of symptoms varies between these types and, indeed, within each type and it is beyond the scope of this brief overview to describe symptoms in detail. People with a personal concern about EB should consult their doctor , in the first instance, for an explanation of their form of EB.
In general terms, EB causes blisters which may be restricted to specific areas, for example hands or feet, or may affect large areas of the body. In the milder forms the blisters heal normally without leaving permanent damage to the skin. In other forms, the blisters heal with scarring which can result in permanent change to the skin, for example fingers may fuse and hands contract, reducing movement. Some forms of Junctional EB are life threatening in infancy.

Does the condition only affect the skin?

Although the effects of EB on the skin are the most visible symptoms, other parts of the body can be affected. The inside of the mouth may blister, causing discomfort and, in some cases, restricted opening. The gullet can also be affected causing difficulties in swallowing and eating. Other mucosal linings may be affected including the eyes and anus. Consequently, a number of different specialists are involved in the care of people with EB and DebRA actively supports specialist treatment centres to provide that care.

Does EB affect mental health or intelligence?

People with EB are just like any other cross section of the population. There is no evidence that EB affects mental health and the same range of intelligence is found amongst people with EB as in any other group. The overwhelming majority of children are best placed in mainstream schooling where they can receive a broadly based education alongside their friends and neighbours.

Is EB infectious or contagious?

EB is neither infectious or contagious and other people cannot "catch" EB from someone with the condition. There is no risk to other people from normal activities such as swimming.

Is EB hereditary?

EB is a genetic condition which is passed on from parents to children. Different forms of EB are passed on in different ways. In some types one parent has EB and it is passed on directly to some of the children. In these cases there is a one in two chance in each pregnancy of the child having the form of EB which the parent has.Other types are transmitted in a more complicated manner, known as recessive inheritance. In this case both parents will be carrying the gene for the disorder but will not themselves ever be affected, i.e. they are carriers. Where this is the case, there is a one in four chance in each pregnancy of the child having EB and a one in two chance that the child will be an unaffected carrier. These "carrier children" will only face the risk of having an affected child themselves in adult life in the unlikely event that their partner is also a carrier.

 

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