Keratosis follicularis spinulosa decalvans

MONDO:0000136

Keratosis 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.

Also known as: keratosis pilaris decalvans

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Sub-types

Keratosis follicularis spinulosa decalvans, autosomal dominant (0) Keratosis follicularis spinulosa decalvans, X-linked (0)

Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Skin disorder (132) Inborn errors of metabolism (45) Human disease (14) Hereditary skin disorder (6) Keratosis (4) Disease of genetic or genomic mechanism (2) Keratosis pilaris (2)

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