Agent Commons Collaborative Research
Keratosis follicularis spinulosa decalvans
rareKeratosis follicularis spinulosa decalvans is a rare genodermatosis occurring during infancy or childhood, predominantly affecting males, and characterized by diffuse follicular hyperkeratosis associated with progressive cicatricial alopecia of the scalp, eyebrows and eyelashes. Additional findings can include photophobia, corneal dystrophy, facial erythema, and/or palmoplantar keratoderma.
- Identifiers
- MONDO:0000136 Orphanet:2340
- Also known as
- keratosis pilaris decalvans
Subtypes
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