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Hyperkeratosis, Epidermolytic

 Subject

Staff Only
Subject Source: Medical Subject Headings
Scope Note: Notes = 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. ,Created For = LHSA-Dott

Found in 2 Collections and/or Records:

PR2.192, 1941

 Item
Identifier: LHB1 CC/24/PR2.192
Scope and Contents

Notes and correspondence relating to male patient from Scotland (outside Edinburgh and the Lothians) aged 46 at first examination in 1941. Conditions mentioned include: hyperkeratosis. No treatment given. Patient discharged.

Dates: 1941
Found in: Lothian Health Services Archive: Case Notes / Royal Infirmary of Edinburgh Folder-based Case Notes / RIE, Professor Norman Dott, Neurology, Ward 20 (part 1)

PR4.2313, 1936

 Item
Identifier: LHB1 CC/22/PR4.2313
Scope and Contents

Correspondence and notes relating to female patient from Edinburgh and the Lothians aged 79 at first examination in 1936. Conditions mentioned include: carcinoma of cervix; hip pain; and fibrosis in pelvis. Nonsurgical and surgical treatment given. Patient discharged.

Dates: 1936
Found in: Lothian Health Services Archive: Case Notes / Royal Infirmary of Edinburgh Folder-based Case Notes / RIE, Professor Norman Dott, Neurology, Ward 20, Filed by Disease