Epidermolysis bullosa

even the slightest physical contact will damage his or her skin. Many children are born with many different diseases. One of the rarest and difficult diseases is Epidermolysis Bullosa, a rare skin disease. Even though this is a rare disease, there is a tremendous amount of knowledge to it and many researchers looking for a cure. Epidermolysis is in a group of inherited diseases that are characterized by blistering lesions on the skin’s surface and in the mucous membranes.

Epidermolysis Bullosa also known as E.B. is generally an inherited connective tissue disease. This disease is evident at birth or soon there after. It causes large fluid filled blisters, in the skin and mucosal membranes. Chaffing or even increase in room temperature may cause these blisters to form. E.B. affects an estimated 50 in 1 million live births. The disease has been known to affect every racial and ethnic group and is found in both males and females all over the world. The disease has

There are four main types of Epidermolysis Bullosa, all can be fatal and they affect infants and children. Each case is different but all of them are extremely painful. Each one ranges from a form of a mild case to severe case and sometimes even death. The four types of Epidermolysis Bullosa include Dystrophic Epidermolysis Bullosa, Epidermolysis Bullosa Simplex, Junctional Epidermolysis Bullosa and Epidermolysis Bullosa Acquista. Each one mentioned above is very different form the other. Each one

Epidermolysis Bullosa, also referred as “EB” is a very dangerous disease. It can be inherited from parents. It is a common disorder that can affect your skin. EB is a “life threatening” disease (Fallon). It can be inherited from a dominant gene or a recessive gene. A “mutation in the COL7A1 gene” can easily cause EB (Pausch). This deadly disease affects about 50,000 people in the United States. Children with this disorder can “lose fingers and toes” (Ezzell).Sometimes, it can affect lungs, the esophagus

there are a few problems that may occur or it can be life threatening. This disease is called Epidermolysis Bullosa. Epidermolysis Bullosa is a genetic disorder that causes the skin to blister even with the slightest force. Epidermolysis Bullosa is found in three different types. Each are caused by different genetic mutations. The most common form of Epidermolysis Bullosa (EB) is Epidermolysis Bullosa simplex (EBS). The less common types of EB

advanced practice nurses have the ability to guide patients in evaluating what they read online. Can these sources provide reliable and appropriate medical advice? The Dystrophic Epidermolysis Bullosa Research Association of America (Debra.org) is a website dedicated to educating the public about Epidermolysis Bullosa (EB). EB is a rare genetic heterogeneous disorder that affects the connective tissue of the skin. The body is unable to produce the appropriate protein and keratin to provide strength

butterfly wings? Do you recall how fragile they were? Now imagine your very own skin being that fragile. This is exactly the case in 7 year - old Hassan’s life. Hassan was diagnosed with a rare genetic disease, at a week old, called epidermolysis bullosa. Epidermolysis bullosa is an incurable disease that causes blisters and erosion of the skin. This disease has affected over 500,000 people worldwide, while 40% of patients die before adolescence. Hassan luckily, was diagnosed and treated in Germany. In

Epidermolysis Bullosa, otherwise called butterfly ailment, is a hereditary skin condition. The skin of patients with this malady is as delicate as the wings of a butterfly. It rankles effectively because of minor harm or grinding, for example, rubbing or scratching. Besides, the patients create endless injuries that are not recuperating and their fingers and toes wire, for instance. The condition is created by a change of the quality COL7A1, which contains the outline for the protein collagen VII

Epidermolysis Bullosa (EB) is classified as a category of bullous, or blistering, disorders that affect a person is they undergo any type of strain to the body. It is a rare inherited disease that affects the keratin in the cells which allow them to have rigidity and strength to protect the body from the environment (Columbe, P.A. et. al). A lack, or mutation, of keratin within the cells causes the epidermis to be susceptible to complete destruction or damage to the cells with even minor damage placed

and suffering. This awful nightmare is epidermolysis bullosa, a rare genetic disorder for which there is no cure. Epidermolysis bullosa is the designation given to a group of hereditary diseases that cause the skin to blister and peel off as a result of even the mildest trauma. The origin of the name is easy to determine. The epidermis is the outer layer of skin; “bullosa” is another term for blister; “lysis” means breakdown. Therefore, epidermolysis bullosa is the breaking down and blistering of