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.

Descriptor ID	D016108
MeSH Number(s)	C16.131.831.493.160 C16.320.850.275.160 C17.300.200.367 C17.800.804.493.160 C17.800.827.275.160 C17.800.865.410.160
Concept/Terms	Epidermolysis Bullosa Dystrophica Epidermolysis Bullosa Dystrophica Bullosa Dystrophica, Epidermolysis Bullosa Dystrophicas, Epidermolysis Dystrophica, Epidermolysis Bullosa Dystrophicas, Epidermolysis Bullosa Epidermolysis Bullosa Dystrophicas Epidermolysis Bullosa, Dystrophic Dystrophic Epidermolysis Bullosa Bullosa, Dystrophic Epidermolysis Bullosas, Dystrophic Epidermolysis Dystrophic Epidermolysis Bullosas Epidermolysis Bullosas, Dystrophic Hallopeau-Siemens Disease Hallopeau-Siemens Disease Hallopeau Siemens Disease Epidermolysis Bullosa Dystrophica, Autosomal Recessive Dystrophic Epidermolysis Bullosa, Autosomal Recessive Epidermolysis Bullosa Dystrophica, Recessive Epidermolysis Bullosa Dystrophica, Hallopeau-Siemens Type Epidermolysis Bullosa Dystrophica, Hallopeau Siemens Type Cockayne-Touraine Disease Cockayne-Touraine Disease Cockayne Touraine Disease Epidermolysis Bullosa Dystrophica, Cockayne-Touraine Type Epidermolysis Bullosa Dystrophica, Cockayne Touraine Type Epidermolysis Bullosa Dystrophica, Dominant Cockayne-Touraine Type Epidermolysis Bullosa Cockayne Touraine Type Epidermolysis Bullosa

Below are MeSH descriptors whose meaning is more general than "Epidermolysis Bullosa Dystrophica".

Below are MeSH descriptors whose meaning is related to "Epidermolysis Bullosa Dystrophica".

Below are MeSH descriptors whose meaning is more specific than "Epidermolysis Bullosa Dystrophica".