Adult epidermolysis bullosa (EB) service

Managing your skin condition

Epidermolysis bullosa (EB) is a rare inherited skin disorder which causes the skin of affected people to be excessively fragile and blister at the slightest knock or rub. There are a number of different types of EB. Some types can cause hands and feet to blister, whilst others can affect larger areas of the skin, significant scarring and internal complications.

Our service

We are one of two national centres for the diagnosis and clinical care of adults with EB. St Thomas’ is a leading centre for translational and clinical research in EB.

The national EB diagnostic laboratory is based within our department. Here we undertake analysis of skin biopsy specimens, genetic testing for EB and prenatal diagnosis of severe forms of EB.

Our team works closely with colleagues from dermatology, plastic surgery, specialist nursing, dentistry, interventional radiology, cancer services, dietetics, the eye department, physiotherapy, occupational therapy, psychotherapy (PDF 115Kb) and foot health.

We also work closely with the genetic skin disease group at King's College London.

Research

Our department is actively involved in clinical research, aiming to continually improve the treatment of EB.

Watch this video of our EB specialist Professor John McGrath speaking to Damian Lewis about the condition and his research.

Contact

Tel: 020 7188 6399

For our clinic locations, please see the patients page.

SKIN, a history

Read more about epidermolysis bullosa and new treatments being trialled in the 'SKIN, a history' book using our page turning software or download chapter 2 (PDF 3.5Mb).