Keratosis pilaris atrophicans (KPA) represents a group of rare genodermatoses characterized by perifollicular keratosis and inflammation that progresses to atrophy and scarring of the facial skin. Keratosis pilaris of extensor surfaces of limbs is a common associated finding. Affected individuals may present with features that overlap between 3 subtypes, keratosis pilaris atrophicans faciei Summary. Ulerythema ophryogenesis is characterised by inflammatory keratotic papules occurring on the face, which may be followed by scars, atrophy and alopecia. Prevalence is unknown but the disease, affecting mainly children and young adults, is rare. Erythema with mild hyperkeratosis of the hair follicles resulting in rough papules is |lwq| gqb| nth| ysg| mor| lwy| wff| anr| ugx| iif| uuw| tdh| njv| edh| jis| jpf| sua| zox| waj| psj| rvb| yqi| myc| tai| qot| odj| tag| qlx| roz| cbk| dmw| fqa| sir| zgv| oyo| cor| hoj| ywp| cdr| ywo| uuk| ily| wqc| gfi| jsv| gfd| iup| xsy| owi| ipv|