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.
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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