Effects of Epidermolysis Bullosa (skin disorder) on the body

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Tinea versicolor is a skin disorder that causes the skin to become fragile and easily bruised. In children with severe symptoms, it can significantly affect daily life and can be life-threatening. Parents can take care of children with Tinea versicolor with appropriate methods to relieve symptoms and make daily life more convenient for the child, such as feeding the child iron-rich foods and applying lotion regularly. Epidermolysis Bullosa is divid into 5 types according to the layer of skin that is affect:

Epidermolysis Bullosa Simplex (EBS)

It is a type of blistering disease that usually occurs on the top layer of the skin, the epidermis. Can be on the palms of the hands or soles of the feet. It is consider the most common form of dermatitis that begins in infants. About 70 percent of people with this type of dermatitis will have milder symptoms than those with other types of dermatitis.

Dystrophic Epidermolysis Bullosa (DEB)

Children with this type of chrysalis will develop symptoms in the dermis, where the skin does not adhere together due to a lack of collagen to hold it together คาสิโนออนไลน์ UFABET ฝากถอนรวดเร็ว เริ่มต้นเล่นง่าย. In some cases, the condition may not show symptoms until childhood.

Junctional Epidermolysis Bullosa (JEB)

It is a lesion that occurs in the basement membrane, which is the layer of skin between the dermis and epidermis. Up to 5 percent of people are at risk of developing this form of bulging skin, and it is consider the most severe form of bulging skin.

Kindler Syndrome

People with this type of skin disorder or blister disease have skin discoloration when exposed to sunlight due to lesions in different layers of the skin, resulting in a variety of symptoms.

Epidermolysis Bullosa Acquisita

This type of blistering disease occurs in areas that are easily injure, such as the hands, feet, knees, elbows, or buttocks. The blister, sometimes with mucus, forms around the mouth, nose, and eyes. This type of lesion is not genetic and usually occurs in adults.