Epidermolysis bullosa (EB) is an inherited, heterogeneous group of rare genetic dermatoses
characterized by mucocutaneous fragility and blister formation, inducible by often minimal …

Based upon case reports and small case series, it has been known for many years that
some types and subtypes of inherited epidermolysis bullosa (EB) may be at risk for …

Background Inherited epidermolysis bullosa (EB) comprises a highly heterogeneous group
of rare diseases characterized by fragility and blistering of skin and mucous membranes …

Background Inherited epidermolysis bullosa (EB) comprises a group of rare disorders that
have multi-system effects and patients present with a number of both acute and chronic pain …

Background: Portions of the gastrointestinal (GI) tract may be severely involved in patients
with inherited epidermolysis bullosa (EB). Evidence-based data are lacking as to the …

Background Epidermolysis bullosa (EB) is a group of inherited disorders characterized by
skin and mucous membrane fragility. Gastrointestinal (GI) complications have been …

Post-esophageal atresia anastomotic strictures and post-corrosive esophagitis are the most
frequent types of cicatricial esophageal stricture. Congenital esophageal stenosis has been …

Dystrophic epidermolysis bullosa (DEB) is a genetic skin disorder affecting skin and nails
that usually presents at birth. DEB is divided into two major types depending on inheritance …

Interventions Weber-Cockayne EB simplex Lesions, usually confined to feet and hands,
especially in hot weather, often severely limit mobility. Frequently painful defecation± …

AIM OF THE STUDY: To assess the efficacy and safety of endoscopic balloon dilatation of
esophageal strictures in children. MATERIAL AND METHODS: Design: retrospective case …