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Junctional Epidermolysis Bullosa (Epidermolysis Bullosa Letalis) Summary

167 relevant articles (3 outcomes, 17 trials/studies) found for this Disease

Description: Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is characterized by generalized blister formation, extensive denudation, and separation and cleavage of the basal cell plasma membranes from the basement membrane.

Also Known As: Epidermolysis Bullosa Letalis; Epidermolysis Bullosa, Junctional; Epidermolysis Bullosa Progressiva; Herlitz's Disease; Herlitz Disease Show All >>

Key Drugs and Agents for Junctional Epidermolysis Bullosa

Efficacy Chart >>
Drugs and Important Biological Agents (IBA) related to treatments:
  1. kalinin : 2 outcomes 6 studies in 75 results : IBA
  2. Hematoxylin (Haematoxylon) : 1 outcome 1 study in 1 result : IBA
  3. Eosine Yellowish-(YS) (Eosin) : 1 outcome 1 study in 1 result : IBA
  4. Phenytoin (Dilantin) : 1 outcome in 4 results : FDA 9 Generic
  5. Laminin (Merosin) : 2 studies in 17 results : IBA
  6. Nonsense Codon (Nonsense Mutation) : 2 studies in 15 results : IBA
  7. DNA (Deoxyribonucleic Acid) : 2 studies in 7 results : IBA
  8. Antigens : 1 study in 16 results : IBA
  9. collagen type XVII (collagen XVII) : 1 study in 15 results : IBA
  10. Integrin beta4 : 1 study in 12 results : IBA
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Diseases Related to Junctional Epidermolysis Bullosa

  1. Blister (Bulla)
  2. Syndrome
  3. Adhesions
  4. Skin Diseases
  5. Epidermolysis Bullosa Dystrophica (Dystrophic Epidermolysis Bullosa)
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Key Therapies for Junctional Epidermolysis Bullosa

Efficacy Chart >>
  1. Transplants (Transplant) : 1 result
  2. Hematopoietic Stem Cell Transplantation : 1 result
  3. Artificial Skin : 1 result
  4. Skin Transplantation (Skin Grafting) : 1 result
  5. Homologous Transplantation (Allograft) : 1 result
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