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keratosis follicularis spinulosa decalvans

Disease Summary
Associated Targets (3)
Tbio

3


Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0000136:  keratosis follicularis spinulosa decalvans
DC:0000550: 
GARD:0006829: 
Orphanet:2340: 
SCTID:238626006: