Article
[Hereditary epidermolysis bullosa: towards classification and genetic counseling based upon identification of molecular defects].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie - 1 Nov 1994
Hovnanian A, de Prost Y
Abstract excerpt
Inherited epidermolysis bullosa (EB) includes three main types depending on the precise ultrastructural level at which the split responsible for the blistering occurs; 1) simplex EB (SEB) located at the level of the basal cells; 2) junctional EB (JEB) located in the lamina lucida; 3) dystrophic E...
Topics
- Cell Adhesion Molecules
- Collagen
- Epidermolysis Bullosa
- Genetic Counseling
- Humans
- Infant, Newborn
- Keratins
- Molecular Biology
- Mutation
- Kalinin
