Hyperkeratosis, Epidermolytic
A form of congenital ichthyosis inherited as an autosomal dominant trait and characterized by ERYTHRODERMA and severe hyperkeratosis. It is manifested at birth by blisters followed by the appearance of thickened, horny, verruciform scales over the entire body, but accentuated in flexural areas. Mutations in the genes that encode KERATIN-1 and KERATIN-10 have been associated with this disorder.
推出的年份: 1993(1979)
树号: C16.131.831.512.400.375, C16.320.850.400.375, C16.614.492.400.375, C17.800.428.333.250.375, C17.800.804.512.400.375, C17.800.827.400.375
MeSH 单一 ID: D017488
进入的组:
Epidermolytic Hyperkeratoses
Hyperkeratoses, Epidermolytic
Bullous Congenital Ichthyosiform Erythroderma
Congenital Bullous Ichthyosiform Erythroderma
Ichthyosiform Erythroderma, Bullous Congenital
Epidermolytic Ichthyosis
Bullous Ichthyosiform Erythroderma Congenital
Bullous Erythroderma Ichthyosiformis Congenita of Brocq
Bullous Ichthyosiform Erythroderma
Bullous Ichthyosiform Erythrodermas
Erythroderma, Bullous Ichthyosiform
Erythrodermas, Bullous Ichthyosiform
Ichthyosiform Erythroderma, Bullous
Ichthyosiform Erythrodermas, Bullous
Epidermolytic Hyperkeratosis
Bullous Erythroderma Ichthyosiforme
Erythroderma Ichthyosiforme, Bullous
Bullous Erythroderma Ichthyosiformes
Erythroderma Ichthyosiformes, Bullous
Ichthyosiforme, Bullous Erythroderma
Ichthyosiformes, Bullous Erythroderma
Congenital Ichthyosiform Erythroderma, Bullous
早前的内容:
Ichthyosiform Erythroderma, Congenital (1991-1992)
Ichthyosis (1966-1992)
Keratosis (1972-1992)
Skin Diseases, Vesiculobullous (1972-1992)
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