Epidermolysis Bullous Congenital Summer

Epidermolysis Bullous Congenital Summer: Rare genetic disease

Congenital epidermolysis bullosa, also known as Weber-Cockayne syndrome, is a rare genetic disorder characterized by the formation of blisters and ulcers on the skin and mucous membranes. This hereditary disease belongs to the group of epidermolysis, which is characterized by damage to skin cells and their failure.

Congenital summer epidermolysis bullosa usually manifests itself in early childhood, often already from the first months of a newborn’s life. The main symptom of this disease is the formation of blisters and ulcers on the skin, especially on areas subject to friction or mechanical irritation such as the elbows, knees, feet and hands. The blisters can vary in size and are often painful. The cause of these blisters is associated with a violation of the structure and functioning of the skin.

In addition, patients with epidermolysis bullosa congenita may also experience insufficient strength of nails and hair, as well as problems with teeth and mucous membranes. The skin of patients with this condition is usually very sensitive and susceptible to infection, which can lead to complications.

The cause of congenital epidermolysis bullosa is associated with