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.
推出的年份: 1991
树号: 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
MeSH 单一 ID: D016108
进入的组:
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
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 Type Epidermolysis Bullosa
Cockayne Touraine Type Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica, Dominant
Epidermolysis Bullosa Dystrophica, Cockayne-Touraine Type
Epidermolysis Bullosa Dystrophica, Cockayne Touraine Type
早前的内容:
Epidermolysis Bullosa (1966-1990)
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