Other epidermolysis bullosa digital illustration

Other epidermolysis bullosa Save


ICD-10 code: Q81.8

Disease category: Q81: Epidermolysis bullosa

Understanding Other Forms of Epidermolysis Bullosa
Epidermolysis bullosa (EB) is a rare genetic disorder that affects the skin's ability to adhere to the body. This results in the formation of blisters and painful sores on the skin, which can lead to secondary infections and scarring. While there are several types of EB, this article will focus on the other forms of EB.
  • Dystrophic Epidermolysis Bullosa (DEB)
    DEB is a rare form of EB that affects the skin, nails, and mucous membranes. It is caused by a mutation in the COL7A1 gene, which produces a protein called collagen type VII. This protein is responsible for anchoring the skin to the body's underlying tissues. Without it, the skin becomes fragile, leading to blistering and open sores. DEB can range from mild to severe, with some patients experiencing scarring and deformities.
    Epidermolysis Bullosa Simplex (EBS)
    EBS is the most common form of EB, affecting the skin's outermost layer. It is caused by a mutation in the genes that produce keratins, which are proteins that give the skin its strength and elasticity. EBS can range from mild to severe, with some patients experiencing blistering and open sores. However, in most cases, the blisters heal without scarring.
    Junctional Epidermolysis Bullosa (JEB)
    JEB is a rare form of EB that affects the skin, mucous membranes, and other tissues. It is caused by a mutation in one of the genes that produce laminin, a protein that anchors the skin to the underlying tissues. Without laminin, the skin becomes fragile, leading to blistering and open sores. JEB can range from mild to severe, with some patients experiencing scarring and deformities.
  • While there is no cure for other forms of EB, there are treatments available to manage the symptoms. These include wound care, pain management, and infection prevention. Patients with severe forms of EB may require specialized medical care, including nutritional support and surgery. It is important for patients with other forms of EB to work closely with their healthcare providers to manage their symptoms and prevent complications. Additionally, patients and their families may benefit from support groups and counseling to help them cope with the emotional and physical challenges of living with EB.

    1. References:
      • National Institute of Arthritis and Musculoskeletal and Skin Diseases. (2016). Epidermolysis Bullosa. Retrieved from https://www.niams.nih.gov/health-topics/epidermolysis-bullosa
      • Genetics Home Reference. (2021). Epidermolysis bullosa

        Treatment of Other epidermolysis bullosa:

        Treatment Options for Other Epidermolysis Bullosa
        Epidermolysis bullosa (EB) is a rare genetic condition that affects the skin and mucous membranes. It is caused by mutations in genes that produce proteins necessary for skin and tissue integrity. There are several types of EB, and each has its own specific symptoms and treatment options. This article will focus on treatment options fo...

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