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A Case of Epidermolytic Hyperkeratosis / 대한피부과학회지
Korean Journal of Dermatology ; : 507-510, 1985.
Article in Korean | WPRIM | ID: wpr-81127
ABSTRACT
Epidermolytic hyperkeratosis, previously called bullous congenital ichthyosiform erythroderma is a dominantly inherited disorcler and usually manifested by blisters at or shortly after birth. We report a case of epidermolytic hyperkeratosis in 9 year old girl vrho developed generalized erythema & easily eroded vesicles at birth. Later the skin lesions progresed to characteristic thick, grayish-dark brown verruform cais, affecting predominantly flexural and intertriginous areas. Fiistologic findings show typical granular degeneration.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Skin / Blister / Hyperkeratosis, Epidermolytic / Cytochrome P-450 CYP1A1 / Parturition / Erythema Limits: Child / Female / Humans Language: Korean Journal: Korean Journal of Dermatology Year: 1985 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Skin / Blister / Hyperkeratosis, Epidermolytic / Cytochrome P-450 CYP1A1 / Parturition / Erythema Limits: Child / Female / Humans Language: Korean Journal: Korean Journal of Dermatology Year: 1985 Type: Article