: MeSH: Epidermolysis Bullosa Dystrophica

Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Vesiculobullous > Epidermolysis Bullosa > Epidermolysis Bullosa Dystrophica

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Epidermolysis Bullosa > Epidermolysis Bullosa Dystrophica

Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Epidermolysis Bullosa > Epidermolysis Bullosa Dystrophica

Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Epidermolysis Bullosa > Epidermolysis Bullosa Dystrophica

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Epidermolysis Bullosa > Epidermolysis Bullosa Dystrophica

Skin and Connective Tissue Diseases > Connective Tissue Diseases > Collagen Diseases > Epidermolysis Bullosa Dystrophica

Epidermolysis Bullosa Dystrophica

Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in COLLAGEN TYPE VII, a major component fibrils of BASEMENT MEMBRANE and EPIDERMIS.

http://data.loterre.fr/ark:/67375/JVR-Z27VX1R7-C

RDF/XML TURTLE JSON-LD Created 2/12/90, last modified 6/18/15

Loterre