ED56ICD-11 MMS 2026-01
Keratosis pilaris
Description
Keratosis pilaris is a very common abnormality of keratinization characterised by keratinous plugging of follicular orifices with varying degrees of perifollicular erythema. It is seen in up to half of normal children and in three quarters of children with ichthyosis vulgaris. The sides of the face and the extensor surfaces of the upper arms are sites of predilection. Autosomal dominant inheritance can often be demonstrated. In some variants atrophy or pigmentation may be more prominent than keratosis.
Index terms
- Keratosis pilaris
- Erythromelanosis follicularis faciei
- Keratosis pilaris atrophicans
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- Ulerythema ophryogenes
- Ulerythema ophryogenis
- ulerythema, unspecified
- Atrophoderma vermiculatum
- Folliculitis ulerythematosa reticulata
- Honeycomb atrophy of face
- Vermiculate atrophoderma of face
- Keratosis follicularis spinulosa decalvans
Sibling codes
Foundation entity
Part of: 14: Diseases of the skin