Epidermolysis Bullosa Causes, Symptoms, Diagnosis and Treatment


What is Epidermolysis Bullosa?

Epidermolysis bullosa (EB) is a group of inherited connective tissue diseases that cause blisters in the skin and mucosal membranes.

The condition usually shows up in infancy or early childhood. Some people don’t develop signs and symptoms until adolescence or early adulthood.

Epidermolysis bullosa has no cure, though mild forms may improve with age.

Treatment focuses on addressing the symptoms and preventing pain and wounds.

Severe forms may cause serious complications and can be fatal.

Causes of Epidermolysis Bullosa:

Epidermolysis bullosa is usually inherited. Researchers have identified more than a dozen genes involved with skin formation that, if defective, may cause a type of epidermolysis bullosa.

The main types of epidermolysis bullosa are:

Symptoms of Epidermolysis Bullosa:

Epidermolysis bullosa exhibits the following signs and symptoms:

Diagnosis of Epidermolysis Bullosa:

The following tests are conducted in order to confirm the diagnosis of epidermolysis bullosa:

Treatment of Epidermolysis Bullosa:

Treatment of epidermolysis bullosa aims to prevent complications and ease the pain of the blisters with appropriate wound care.

However, the condition often progresses despite treatment, sometimes causing serious complications and death.

The following treatment options are available:

By : Natural Health News

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